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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1448383생성일: 2026년 10월 25일

Sodium Hydroxide → HCID 178431925, 화합물

https://huagongshe.com/reaction/1448383

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물(2-(Azidomethyl)phenyl)acetic acidHCID 3016229—
반응물HCID 178431949HCID 178431949—
용매Oxolane--water (1/1)HCID 21881883—
생성물HCID 178431925HCID 178431925—

반응 조건

온도0 °C

반응 단계

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 1.0 N 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 aqueous 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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04179511
출처 데이터셋uspto-grants-1979_12
ORD IDord-5ea4051627ff408a8fae01498ee255e3
출처 메모uspto-grants-1979_12