돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2288257생성일: 2026년 10월 27일

Water → (2S)-2-((1-Naphthalenyloxy)methyl)oxirane

https://huagongshe.com/reaction/2288257

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1-NaphtholHCID 7005—
반응물Cesium fluorideHCID 25953—
반응물Benzenesulfonic acid, 3-nitro-, (2S)-2-oxiranylmethyl esterHCID 146490—
용매DimethylformamideHCID 6228—
생성물(2S)-2-((1-Naphthalenyloxy)methyl)oxiraneHCID 14893396.5%

반응 조건

온도0 °C

반응 단계

1-Naphthol (1.0 g) was dissolved in DMF (8 ml) under nitrogen atmosphere and the solution was cooled to 0° C. Cesium fluoride (2.11 g) was added thereto and the mixture was stirred for 1 hour. Then, (S)-glycidyl m-nitrobenzenesulfonate (1.80 g, 99.3% e.e.) was added thereto and the mixture was stirred for 24 hours at the same temperature. After the reaction, water was added to the mixture, the mixture was extracted with ethyl acetate, dried over anhydrous magnesium sulfate, condensed and the residue was subjected to silica gel chromatography (hexane/ethyl acetate; 6:1) to give 1.34 g of (S)-1-(2,3-epoxypropoxy)naphthalene (yield 96.5%, optical purity 99.2% e.e.) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06087512
출처 데이터셋uspto-grants-2000_07
ORD IDord-0b822150599e487ab5c5bf2b5559675d
출처 메모uspto-grants-2000_07