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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 48113생성일: 2026년 10월 24일

1,1,1-Trifluoro-N-phenylmethanesulfonamide → 6-Trifluoromethanesulfonyloxy-1,2,3,4-tetrahydro-naphthalene-2-carboxylic Acid (1S)-1-Methylheptyl Ester

https://huagongshe.com/ko/reaction/48113

반응식

참여 물질

역할이름HCID투입량
반응물1,1,1-Trifluoro-N-phenylmethanesulfonamideHCID 68012—
반응물6-Hydroxy-1,2,3,4-tetrahydro-naphthalene-2-carboxylic Acid (1S)-1-Methylheptyl EsterHCID 60072476—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물6-Trifluoromethanesulfonyloxy-1,2,3,4-tetrahydro-naphthalene-2-carboxylic Acid (1S)-1-Methylheptyl EsterHCID 20632179—

반응 단계

To a solution 6-hydroxy-1,2,3,4-tetrahydro-naphthalene-2-carboxylic acid (1S)-1-methylheptyl ester (37) (1 equi.), and N-phenyl trifluoromethanesulfonamide (1 equi.) in dichloromethane (10 mL/mmole), triethylamine (1.5 equi.) was added at −78 C. The reaction mixture was stirred at that temperature for 1 h and at room temperature for 24 h, quenched with water, extracted with ethyl acetate:hexane(1:1), washed with brine, dried over MgSO4, and concentrated in vacuo. Purification by chromatography on silica gel (5% EtOAc/hexanes) gave 6-trifluoromethanesulfonyloxy-1,2,3,4-tetrahydro-naphthalene-2-carboxylic acid (1S)-1-methylheptyl ester (45), as a colorless oil (92%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06703082B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-7f374d178bd64287acc3ecbfc2555bf1
출처 메모uspto-grants-2004_03