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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 456858생성일: 2026년 10월 27일

Triethylamine → 1-(3-Nitrophenyl)ethyl methanesulfonate

https://huagongshe.com/reaction/456858

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물alpha-Methyl-3-nitrobenzenemethanolHCID 223135—
용매DichloromethaneHCID 6344—
생성물1-(3-Nitrophenyl)ethyl methanesulfonateHCID 1936967771%

반응 조건

온도20 °C

반응 단계

A solution of 4.63 ml (59.8 mmol) of methane sulphonyl chloride diluted with 20 ml of dichloromethane is added dropwise to a solution of 10 g (59.8 mmol) of 3-nitrophenylethanol and 8.31 ml (59.8 mmol) of triethylamine in 120 ml of dichloromethane, cooled down with an ice bath. Agitation is maintained for 1 hour at 0° C. and for 2 hours at 20° C. The reaction mixture is then concentrated under vacuum and the residue is taken up in 125 ml of ethyl acetate and 100 ml of water. After agitation and decantation, the organic phase is washed successively with 100 ml of water and 100 ml of salt water. The organic solution is dried over magnesium sulphate, filtered and concentrated under vacuum. The evaporation residue is purified on a silica column (eluent heptane/ethyl acetate 6/4) and the pure fractions are collected and evaporated in order to produce a yellow oil with a yield of 71%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07186752B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-5b5db0e03e8d49e280655dd9b2a847ba
출처 메모uspto-grants-2007_03