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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1409553생성일: 2026년 10월 27일

Methanesulfonyl chloride → (1-Phenylcyclopentyl)methyl methanesulfonate

https://huagongshe.com/reaction/1409553

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonyl chlorideHCID 31297—
반응물(1-Phenylcyclopentyl)methanolHCID 123544—
용매DichloromethaneHCID 6344—
생성물(1-Phenylcyclopentyl)methyl methanesulfonateHCID 1943791461.1%

반응 단계

To a solution of (1-phenyl-cyclopentyl)-methanol (11.5 g, 64.34 mmol) in DCM (100 ml) was added TEA (17.5 ml, 130.68 mmol) and followed by methanesulfonyl chloride (MsCl) (8.9 g, 78.4 mmol) was added drop wise at 0° C. and the reaction mixture was stirred at RT for 16 h. After completion of the reaction, it was quenched with water and concentrated. Then the crude product was dissolved in DCM, extracted with DCM and the organic layer was washed with water, and brine and then dried over Na2SO4. The combined organic layer was concentrated to get crude methanesulfonic acid 1-phenyl-cyclopentylmethyl ester (10 g, crude) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08921388B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-087fa2896d7a4b46841ac6d5ff349e6f
출처 메모uspto-grants-2014_12