돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2168167생성일: 2026년 10월 25일

Ammonia → (S)-2-amino-1-((S)-2,5-dihydrofuran-2-yl)ethanol

https://huagongshe.com/reaction/2168167

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물MethanolHCID 887—
반응물Ammonium ChlorideHCID 25517—
반응물(3R,3aS,6S,6aS)-6-Bromohexahydrofuro[3,2-b]furan-3-yl 4-methylbenzenesulfonateHCID 59343394—
촉매ZincHCID 23994—
용매WaterHCID 962—
용매IsopropanolHCID 3776—
생성물(S)-2-amino-1-((S)-2,5-dihydrofuran-2-yl)ethanolHCID 55280978—

반응 조건

온도75 °C

반응 단계

A solution of ammonium chloride (560 mg, 10.5 mmol) in water (7 mL) was added to a solution of bromotosylate (46) (2.86 g, 7.88 mmol) in propan-2-ol (14 mL) under argon. Zinc dust (560 mg, 8.67 mmol) was then added in portions over 4 minutes then the suspension stirred for 16 hours before filtering through celite in vacuo. The filter cake was washed with diethyl ether (60 mL). Hydrochloric acid (1M, 60 mL) was added to the filtrate then the organic phase separated. The aqueous layer was extracted with diethyl ether (60 mL) then the combined organic phase was washed with brine (60 mL), then dried (MgSO4), filtered and reduced in vacuo. The residue was dissolved in ammonium hydroxide (18 mL) and a solution of ammonia in propan-2-ol (12 mL, 2.0M, 24 mmol) then divided into three equal portions and heated in sealed tubes at 75° C. for 16 hours. The mixtures were combined using methanol then the solvents were removed in vacuo. The residue was azeotroped with diethyl ether (3×10 mL) to obtain (S)-2-amino-1-((S)-2,5-dihydrofuran-2-yl)ethanol which was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09045492B2
출처 데이터셋uspto-grants-2015_06
ORD IDord-69c0f41f04de4320bd64ba2e5d2b6b1e
출처 메모uspto-grants-2015_06