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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2371751생성일: 2026년 10월 27일

Ethyl chloroformate → Enrofloxacin Ethyl Ester

https://huagongshe.com/reaction/2371751

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl chloroformateHCID 10928—
반응물EnrofloxacinHCID 71188—
용매ChloroformHCID 6212—
용매TriethylamineHCID 8471—
생성물Enrofloxacin Ethyl EsterHCID 11760871—

반응 조건

온도-20 °C

반응 단계

100 parts by weight of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(4-ethyl-1-piperazinyl)-3-quinoline-carboxylic acid were dissolved in 300 parts by volume of anhydrous chloroform, and 33.2 parts by weight of triethylamine were added. A solution of 37.7 parts by weight of ethyl chloroformate in 100 parts by volume of anhydrous chloroform was added dropwise to this mixture at -20° C. in the course of 30 minutes, and the mixture was stirred for a further 30 minutes at -20° C. and was then stirred overnight at room temperature. After extraction with twice 300 parts by volume of water, 400 parts by volume of water were added to the organic phase. The pH was adjusted to 5 with glacial acetic acid (consumption approximately 15 parts by volume), and the chloroform was removed by distillation under a water pump vacuum. The pH of the aqueous solution was adjusted to 8.9 with half-concentrated potassium hydroxide solution (consumption approximately 70 parts by volume), and the mixture was stirred overnight at room temperature. The product was filtered off with suction, washed with 500 parts by volume of water and dried overnight at 70° C. in a vacuum drying cabinet.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05095112
출처 데이터셋uspto-grants-1992_03
ORD IDord-3b0346ad6e3648c1a25d010ceebd46c1
출처 메모uspto-grants-1992_03