Bromo propionic acid

Propionic acid, 2-bromo-3-(3-indolyl)-methyl ester rearrangement, 4, 279 Propionic acid, 3-(3,4-dimethyoxyphenyl)-dihydrocoumarin synthesis from, 3, 848 Propionic acid, indolyl-synthesis, 4, 232 Propionic acid, 3-(l-indolyl)-sodium salt pyrolysis, 4, 202 Propionic acid, 3-(3-indolyl)-intramolecular acylation, 4, 220, 221 Propionic acid, 3-phenoxy-chroman-4-one synthesis from, 3, 855 Propionic acid, 3-(3-phenylisoxazoI-5-yl)-bromination, 6, 25... 

AI3-52314 a-Bromopropionic acid 2-Bromopropanoic xid 2-Bromopropionic acid EINECS 209-947-6 NSC 172 Propanoic acid, 2-bromo- Propionic acid, 2-bromo... 

Chloro-2,2,3-trifluoropropionic acid has been prepared by permanganate oxidation of 3-chloro-2,2,3-trifluoropropanol which is one of the telomerization products of chlorotrifluoroethylene with methanol. The present procedure is a modification of one reported earlier and is undoubtedly the method of choice for making propionic acids containing 2 fluorine atoms, i.e., 2,2,3,3-tetrafluoropropionic acid, 3,3-dichloro-2,2-difluoropropionic acid, and 3-bromo-2,2,3-trifluoropropionic acid. When preparing 2,2,3,3-tetrafluoropropionic acid from tetrafluoroethylene, it is desirable to use an additional 50 ml. of acetonitrile and externally applied heat to initiate the reaction. 

The member of this class which has been studied most thoroughly is 2-benzylidene-4-methyl-5(2 )-oxazolone (57). This compound may be prepared by ring closure of either 3-bromo-2-phenylacetamido-propionic acid or A-(a-halophenylacetyl)alanine (56) [Eq. (30)]. These reactions presumably proceed via unstable halogeno-5(4IT)-oxazolones, which rapidly lose hydrogen halide. 

Johnson s classic synthesis of progesterone (1) commences with the reaction of 2-methacrolein (22) with the Grignard reagent derived from l-bromo-3-pentyne to give ally lie alcohol 20 (see Scheme 3a). It is inconsequential that 20 is produced in racemic form because treatment of 20 with triethyl orthoacetate and a catalytic amount of propionic acid at 138 °C furnishes 18 in an overall yield of 55 % through a process that sacrifices the stereogenic center created in the carbonyl addition reaction. In the presence of propionic acid, allylic alcohol 20 and triethyl orthoacetate combine to give... 

Propionic acid, 2-iodo-3-nitro-, ethyl ester [Propanoic acid, 2-iodo-3-mtro-, ethyl ester], 65 2//-Pyran, 3,4-dihydro-, 51 2//-PYR AN-2-ONE, 49 2H Pyran 2-one, 5 bromo 5,6-dihydro, 50 27/-PYRAN-2-ONE, 5,6 DIHYDRO-, 49 PYRIDINE, 2,3,4,5 TETRAHYDRO, 118 Pyridines, -substituted, 34 a Pyrone-6-carboxyhc acid [2H Pyran-6-Larboxyhc acid 2-oxo ], 51 Pyrroles, 34... 

Tocopheryl)propionic acid (50) is one of the rare examples that the o-QM 3 is involved in a direct synthesis rather than as a nonintentionally used intermediate or byproduct. ZnCl2-catalyzed, inverse hetero-Diels-Alder reaction between ortho-qui-none methide 3 and an excess of <2-methyl-C,<9-bis-(trimethylsilyl)ketene acetal provided the acid in fair yields (Fig. 6.37).67 The o-QM 3 was prepared in situ by thermal degradation of 5a-bromo-a-tocopherol (46). The primary cyclization product, an ortho-ester derivative, was not isolated, but immediately hydrolyzed to methyl 3-(5-tocopheryl)-2-trimethylsilyl-propionate, subsequently desilylated, and finally hydrolyzed into 50. 

The reaction of potassium 3-amino-4-oxo-3,4-dihydroquinazoline-2-thiolate 62 with a-bromophenylacetic acid 63 resulted in the formation of (3-amino-4-oxo-3,4-dihydroquinazolin-2-ylsulfanyl)-phenyl-acetic acid methyl ester 64 which on alkali treatment and subsequent acidification resulted in the synthesis of 2-phenyl- 1-thia-4,4a,9-triaza-anthracene-3,10-dione 65 <1999JCR(S)86>. Similarly, the reaction of potassium 3-amino-5,6-dimethyl-4-oxo-3,4,4a,7a-tetrahydrothieno[2,3- pyrimidine-2-thiolate 66 with a-bromo-ester 67 resulted in the formation of 2-(3-amino-5,6-dimethyl-4-oxo-3,4,4a,7a-tetrahydrothieno[2,3- / pyrimidin-2-ylsulfanyl)-propionic acid ethyl ester 68. Subsequent treatment with alkali followed by acidification resulted in the formation of 2,3,7-trimethyl-3a,9a-dihydro-l,8-dithia-4a,5,9-triazacyclopenta[ ]naphthalene-4,6-dione 69 <2000JHC1161>... 

In a more detailed study, the same esterase P. fluorescens) was again subjected to mutagenesis using the same mutator strain, but also by saturation mutagenesis at selected positions 133a). In addition to 3-phenylbutyric acid ethyl ester (27), 3-bromo-2-methyl-propionic acid methyl ester rac-31) was chosen for the hydrolytic kinetic resolution, with the WT PFE showing an E factor of 12 in favor of the (5)-32. 

Estradiol methylether acetate, or 4-Bromo or 4-Chloroestradiol diacetate 3-( 1 P-Acetoxy-8p-methyl-5p-carboxy-trani-perhydroindanyl-4a) propionic acid C [250]... 

Opening of the dithiazole ring of the imidazolo[4,5-r7 [l,2,3]dithiazole 107 was employed as a key step in a multistep synthesis leading to hydroxamic acid derivatives 108 and 109 which are under investigation as matrix metalloproteinase inhibitors. Following initial reaction of 107 with NaOH treatment with 2-bromo-3-(4-chlorophenyl)propionic acid tert-butyl ester lead to the thioethers 108 from which 109 could be obtained (Scheme 10). <2000W0063197>. 

To the crude mixture of ammonium bromide and /3-bromo-propionic acid, prepared as described on p. 25, from 317 g. of ethylene cyanohydrin, are added 1200 cc. of carbon tetrachloride and 200 cc. of the same solvent which has been shaken with the aqueous distillates the ammonium bromide is filtered off and washed with 200 cc. of carbon tetrachloride. The watery layer, amounting to about 350 cc., is separated and shaken with 100 cc. of carbon tetrachloride. To the united carbon tetrachloride solutions are added 450 cc. of 95 per cent ethyl alcohol and 10 g. of sulfosalicylic acid or phenolsulfonic acid to act as a catalyst (Note 1). 

An early effort to generate a 3-lithiated propionic acid derivative and react it with (external) electrophiles was reported in 1978 [42]. Since simple 3-lithioesters failed to undergo the required reaction, the alkyl carboxylate portion was protected by preceding conversion to the carboxylate anion. Treatment of lithium 3-bromo-propionate with lithium naphthalide generated the desired dilithiated propionic acid, which gave moderate yields of y-hydroxy acid addition products with carbonyl compounds, Eq. (45). 

R = Me or Ph).447 Cyclization of j8-(2-bromo-3-benzo[6]thienyl)-propionic acid with liquid hydrogen fluoride, however, proceeds with... 

Bromination of cinnamic acid with NBS in aq. MeOH gives 2-bromo-3-methoxy-3-phenyl propionic acid, PhCH(0Me)CHBrC02H. At moderately high [H+] the reaction is second-order and independent of [H+], whereas at low [H+] the rate increases with decrease in [H+], Succinimide inhibits the reaction182. 

Reaction of 2-aminopyridines with acrylic acid or methacrylic acid in boiling water for 2-20 hours gave betaine hydrates 262 (R3 = H) in 11-88% yields (Scheme 20) (92KGS80). When 2-aminopyridine reacted with methyl metharylate in acetic acid for 24 hours or 2-aminopyridine and its 5-bromo and 5-chloro derivatives reacted with acrylic acid in boiling toluene for 24 hours or 2-aminopyridine reacted with crotonic acid in boiling toluene for 20 hours, 3-(2-pyridylamino)propionic acid derivatives 263 were the products. When 5-chloro-2-aminopyridine reacted with acrylic... 

Sodium 2-Bromo-2-methyl-propionic acid ethyl ester... 

Bromo propionic acid diclofop-methyl, furalaxyl, metalaxyl, naproanilide, napropamide, see chloro propionic acid... 

Methyl p,P -dibromoisobutyrate Propionic acid, 3-bromo-2-(bromo-methyl)-, methyl ester (8, 9) (22262-60-8)... 

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