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Acetyl Chloride enol acetylation

Enol acetates are readily prepared from saturated ketones by reaction with acetic anhydride alone or diluted, in the presence of acetyl chloride ... [Pg.390]

Enol esterification with acetyl chloride-acetic anhydride gives the A -trien-3-acetate, but reaction with isopropenyl acetate or with hot acetic anhydride-pyridine gives A " -trien-3-acetates. " Since A"" -3-ketones react with Girard reagents, these linear dienones can be separated from A ""-3-ketones. ... [Pg.395]

The most simple l, 4-dithiocin system, which is stable, is the 6-acetoxy derivative 13, which can be synthesized from 1,4-dithiocin-6(57/)-onc (12) by trapping its enolate with acetyl chloride.7 9... [Pg.567]

High antiscorbutic power is also reported to be shown by a derivative of L-ascorbic acid in which the enolic hydroxyl group at C2 is replaced by an amino group. 3,4-Isopropylidene-L-threonic acid (LX), prepared from 5,6-isopropylidene-L-ascorbic acid, is converted into the 2-acetyl-3,4-isopropylidene-L-threonyl chloride (LXI) and this is then allowed to react with the sodium derivative of ethyl malonate. [Pg.110]

Many examples exist where the open chain betaine may be quenched by reagents, giving stable phosphorus compounds with P-C1V = 3. When (180) is reacted with acetyl chloride the open chain enol phosphate (181) is formed. Many interesting O- and N-phosphaspirans are also mentioned in (75BSF407). [Pg.535]

Diketones are converted into pyranones on treatment with malonyl dichloride, involving both C- and O-acylation (63JCS4483). The reaction between benzoylacetone and the acid chloride gives only one pyranone in accordance with a preferred direction of enolization consequent upon the unsymmetrical nature of the diketone a 5-acetyl-6-phenylpyranone results rather than the 5-benzoyl-6-methyl isomer. There is still some uncertainty as to whether the product is the 4-hydroxypyran-2-one (409) or the tautomer, but the former is considered to be the more likely. There is yet further controversy, since... [Pg.811]

N-Acetyl-L-phenylalanylsarcosine amide, 348 O-Acetylserine, 148 N-0 Acyl migrations, 157 Acyl-enzyme, 342-350 Z-0-Acylisoamide, 295 1,4-Addition, 221-242 1,6-Addition, 231 L-Ala-L-Ala-pNA,350 f-Ala-T-Pro-pNA, 350 AicohoT dehydrogenase, 340-341 Aldehydes, 209-211 Aldol condensation, 304-306 2-Alkoxytetrahydrofuran, 86 2-Alkoxytetrahydropyran, 18, 85-90 Alkylation of enamine, 282 Alkylation of enolate, 280 C and 0-Alkylation, 240 O-Alkylbenzohydroximoyl chloride, 155... [Pg.194]


See other pages where Acetyl Chloride enol acetylation is mentioned: [Pg.103]    [Pg.85]    [Pg.651]    [Pg.193]    [Pg.125]    [Pg.231]    [Pg.126]    [Pg.215]    [Pg.330]    [Pg.775]    [Pg.166]    [Pg.178]    [Pg.140]    [Pg.172]    [Pg.350]    [Pg.109]    [Pg.133]    [Pg.182]    [Pg.18]    [Pg.250]    [Pg.872]    [Pg.927]    [Pg.321]    [Pg.911]    [Pg.62]    [Pg.59]    [Pg.467]    [Pg.220]    [Pg.648]    [Pg.85]    [Pg.344]    [Pg.103]    [Pg.83]    [Pg.1860]    [Pg.265]    [Pg.577]    [Pg.345]    [Pg.383]    [Pg.220]    [Pg.648]    [Pg.584]   
See also in sourсe #XX -- [ Pg.19 ]




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