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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 377459생성일: 2026년 10월 24일

Dichloromethane → sarcosine-O-fluorenylmethyl ester hydrochloride salt

https://huagongshe.com/ko/reaction/377459

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Glycine, N-[(1,1-dimethylethoxy)carbonyl]-N-methyl-HCID 83692—
반응물9H-Fluorene-9-methanolHCID 90466—
반응물Bis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
용매Ethyl AcetateHCID 8857—
생성물sarcosine-O-fluorenylmethyl ester hydrochloride saltHCID 13172035473%

반응 단계

To a solution of Boc-sarcosine (30 g, 158 mmole) in 500 mL dichloromethane was added with stirring carbonyl diimidazole (25.7 g, 158 mmole). After 15 minutes, 9-fluorene methanol (29.5 g, 150 mmole) was added and stirring was continued. After 16 hours, the reaction mixture was diluted with 1200 mL ethyl acetate and extracted with 300 mL each of water, 1 M aqueous hydrochloric acid, water, saturated aqueous sodium bicarbonate and brine. The organic phase was dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The resulting oil was dissolved in 500 mL dichloromethane and treated with 100 mL of a 4.0M solution of hydrochloric acid in dioxane. After 12 hours, the title compound was precipitated by pouring the reaction mixture into ether (1000 mL) with vigorous stirring. The precipitate was filtered and dried in vacuo to provide 35 g (73% yield) of the title compound as an off-white powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06025472
출처 데이터셋uspto-grants-2000_02
ORD IDord-f9bc15262fdb481c936390da329f0620
출처 메모uspto-grants-2000_02