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HRID 263746作成日:2026年10月27日

benzhydryl (E)-(2S,3S,5R)-3-(2-chloro-vinyl)-3-methyl-4,4,7-trioxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylate → Sodium (E)-(2S,3S,5R)-3-(2-chloro-vinyl)-3-methyl-4,4,7-trioxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylate

https://huagongshe.com/reaction/263746

反応式

関与物質

役割名称HCID仕込み量
反応物benzhydryl (E)-(2S,3S,5R)-3-(2-chloro-vinyl)-3-methyl-4,4,7-trioxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylateHCID 10742000—
反応物Sodium 2-ethylhexanoateHCID 23672331—
溶媒M-CresolHCID 342—
溶媒Methyl Isobutyl KetoneHCID 7909—
生成物Sodium (E)-(2S,3S,5R)-3-(2-chloro-vinyl)-3-methyl-4,4,7-trioxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylateHCID 86750938—

反応条件

温度50 °C

反応手順

385 mg (0.86 mmol) of benzhydryl (E)-(2S,3S,5R)-3-(2-chloro- vinyl) -3- methyl-4,4,7-trioxo-4-thia- 1-aza-bicyclo [3.2.0]heptane-2-carboxylate are dissolved in 2.3 ml of m-cresol under argon and stirred at 50° C. for 4 hours. Subsequently, the mixture was diluted with 15 ml of isobutyl methyl ketone, treated with 0.50 ml of sodium 2-ethylcaproate (2N solution in ethyl acetate) and extracted three times with 8 ml of water each time. The combined aqueous phases were washed once with 10 ml of isobutyl methyl ketone, lyophilized and the lyophilizate obtained was chromatographed over polymeric hydrophobic gel with water as the eluent. Yield: 57 mg (32%) MS: (M--Na)- 278.2 IR (KBr): 1780, 1626, 1564, 1417, 1329, 1145 cm-1

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05644053
出典データセットuspto-grants-1997_07
ORD IDord-5e606b15b4c5498c94046bd224fef880
出典メモuspto-grants-1997_07