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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 465916생성일: 2026년 10월 23일

Hydrochloric Acid → N-(2-ethoxycarbonyloxy-4-methoxybenzoyl)cysteamine

https://huagongshe.com/ko/reaction/465916

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물CysteamineHCID 6058—
반응물Ethyl chloroformateHCID 10928—
반응물4-Methoxysalicylic AcidHCID 75231—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물N-(2-ethoxycarbonyloxy-4-methoxybenzoyl)cysteamineHCID 1471950989%

반응 조건

온도-15 °C

반응 단계

Under argon atmosphere, 2.84 g of 4-methoxysalicylic acid was dispersed in 45 ml of methylene chloride, and the dispersion was cooled to -15° C. To the dispersion was added 3.76 g of triethylamine and 3.77 g of ethyl chlorocarbonate, and the mixture was agitated for 1.5 hour. To the mixture was added a solution of 1.56 g of cysteamine in 5 ml of methylene chloride, and the mixture was agitated at -15° C. for 2 hours. The reaction mixture was poured into 1N aqueous hydrochloric acid, and extracted with methylene chloride. The organic layer was washed with saturated aqueous solution of sodium chloride, and dried over anhydrous sodium sulfate. The solvent was distilled off in evacuated atomosphere, and the residue was subjected to column chromatography using silica gel. There was obtained 4.50 g of N-(2-ethoxycarbonyloxy-4-methoxybenzoyl)cysteamine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05155106
출처 데이터셋uspto-grants-1992_10
ORD IDord-3ae318039fa6472396b71c8f4c0654bb
출처 메모uspto-grants-1992_10