戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1764379作成日:2026年10月25日

Sodium Hydroxide → HCID 178431925、化合物

https://huagongshe.com/reaction/1764379

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物(2-(Azidomethyl)phenyl)acetic acidHCID 3016229—
反応物HCID 178431949HCID 178431949—
溶媒Oxolane--water (1/1)HCID 21881883—
生成物HCID 178431925HCID 178431925—

反応条件

温度0 °C

反応手順

A stirred suspension of 21.73 g. of 6-amino-2,2-dimethyl-3-(5-tetrazolyl)penam in 400 ml. of a 50:50 mixture of tetrahydrofuran-water is cooled to ca. 0° C. and the pH is adjusted to 7.5 using 1.0N sodium hydroxide. To the solution thus obtained, is added 17.3 g. of 2-(2-azidomethylphenyl)acetic acid (U.S. Pat. No. 3,766,175), followed by 17.4 g. of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride. The pH drops to 5.5. The reaction mixture is then stirred at ambient temperature, at pH 6, for 3 hours. At this point, the bulk of the tetrahydrofuran is removed by evaporation in vacuo, and the residual aqueous phase is extracted with ethyl acetate. The organic extract is discarded and the aqueuos phase is cooled to ca. 0° C. The pH is then adjusted to 2 and the product is extracted into ethyl acetate. The ethyl acetate is dried and evaporated, leaving 34.8 g. of the title compound as a tan solid. IR(CHCl3) 2100, 1790, 1680 and 1515 cm.-1NMR (DMSO-d6): 7.37 (s, 4H), 5.60 (m, 2H), 5.23 (s, 1H), 4.55 (s, 2H), 3.70 (s, 2H), 1.66 (s, 3H) and 1.06 ppm (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04115385
出典データセットuspto-grants-1978_09
ORD IDord-1942deb3eb2647b48a23013105664629
出典メモuspto-grants-1978_09