Erlenmeyer

Erlenmeyer s rule This originally postulated that all unsaturaled alcohols of the types... 

Flasks. Round-bottomed, flat-bottomed, conical (Erlenmeyer) and bolt-head flasks up to a capacity of 2-3 litres are generally fitted with a 524 socket f those from 5 to 100 ml. are available with a 514 or 519 (from 25 ml.) socket. Round- and flat-bottomed flasks exceeding 1 litre in capacity are supplied with 534 necks. Whilst all sizes of sockets can be obtained from the manufacturers, it is usually convenient to limit the socket sizes to a small number (say, 514, 519, 524 and 534), thus per mitting interchangeability with the minimum number of adapters. 

Benzilic acid rearrangement Benzoin reaction (condensation) Blanc chloromethylation reaction Bouveault-Blanc reduction Bucherer hydantoin synthesis Bucherer reaction Cannizzaro reaction Claisen aldoi condensation Claisen condensation Claisen-Schmidt reaction. Clemmensen reduction Darzens glycidic ester condensation Diazoamino-aminoazo rearrangement Dieckmann reaction Diels-Alder reaction Doebner reaction Erlenmeyer azlactone synthesis Fischer indole synthesis Fischer-Speior esterification Friedel-Crafts reaction... 

The apparatus to use is seen in figure 13 which consists of a burette, thermometer, Erlenmeyer flask and a two-holed rubber stopper that has a small V-shaped wedge cut out of one side of the rubber stopper to allow the inside contents to vent. 31.5g of orangy-red fuming nitric acid (see chemicals section) is poured into the Erlenmeyer flask and the rubber stopper with its burette and thermometer is placed on to the... 

H. Erlenmeyer and H. Kiefer. Heir. Chim.. Acta. 28, 0 945i Chem.. Abstr.. 40. 

Erlenmeyer and Schmid (459), in the course of a fundamental comparison between pyridine and its isosteric thiazole structures, prepared the... 

The first identified complexes of unsubstituted thiazole were described by Erlenmeyer and Schmid (461) they were obtained by dissolution in absolute alcohol of both thiazole and an anhydrous cobalt(II) salt (Table 1-62). Heating the a-CoCri 2Th complex in chloroform gives the 0 isomer, which on standirtg at room temperature reverses back to the a form. According to Hant2sch (462), these isomers correspond to a cis-trans isomerism. Several complexes of 2,2 -(183) and 4,4 -dithiazolyl (184) were also prepared and found similar to pyridyl analogs (185) (Table 1-63). Zn(II), Fe(II), Co(II), Ni(II) and Cu(II) chelates of 2.4-/>is(2-pyridyl)thiazole (186) and (2-pyridylamino)-4-(2-pyridy])thiazole (187) have been investigated. The formation constants for species MLr, and ML -" (L = 186 or 187) have been calculated from data obtained by potentiometric, spectrophotometric, and partition techniques. 

This typical behavior of the very unsymmetrical thiazole ring led to a series of studies from the group of H. Erlenmeyer in Basle be studied the H/D exchange of 2,4-dimethyl-5-carboxythia2ole as well as that of similar methylated nitrogen heterocycles (507). The results are shown in Fig. 1-27. 

Erlenmeyer et al. also examined the behavior of 4-methyl-, 4,5-dimethyl-, and 5-methylthiazole in the reaction with benzaldehyde at 160°C in the presence of ZnClj (439, 510) they were able to show that neither the 4- nor 5-methyl groups reacted under these conditions and that the condensation occurred at the sole unsubstituted 2-position (Scheme 114). 

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