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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 342835생성일: 2026년 10월 25일

Triethylamine → methyl N-tert-butoxycarbonylaminomethyl-salicylate

https://huagongshe.com/reaction/342835

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Di-tert-butyl dicarbonateHCID 90495—
반응물Methyl 4-aminomethylsalicylate hydrochlorideHCID 22556073—
용매MethanolHCID 887—
생성물methyl N-tert-butoxycarbonylaminomethyl-salicylateHCID 5455837597.4%

반응 단계

Methyl 4-aminomethylsalicylate hydrochloride (10.9 g, 50 mmoles) was suspended in anhydrous methanol (200 mL) and di-tert-butyldicarbonate (10.9 g, 50 mmoles) and triethylamine (7.0 mL, 50 mmoles) were added. The solid rapidly dissolved with the slow evolution of gas. The reaction mixture was stirred at room temperature for 18 hours under dry nitrogen, then evaporated to dryness to afford a white amorphous mass. This mass was partitioned between ethyl acetate (200 mL) and water (100 mL). The layers were separated, and the ethyl acetate solution was dried over anhydrous sodium sulfate. The solution was filtered and evaporated to a white solid. This solid was crystallized from ethyl acetate/hexanes, filtered, and dried in vacuo to afford 13.7 g (97% yield) of methyl N-tert-butoxycarbonylaminomethyl-salicylate (m.p. 95°-96° C., open capillary, uncorrected).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05859210
출처 데이터셋uspto-grants-1999_01
ORD IDord-ed86b194f7f74cedb942ce9932ec7c4a
출처 메모uspto-grants-1999_01