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HRID 48113作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物1,1,1-Trifluoro-N-phenylmethanesulfonamideHCID 68012—
反応物6-Hydroxy-1,2,3,4-tetrahydro-naphthalene-2-carboxylic Acid (1S)-1-Methylheptyl EsterHCID 60072476—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物6-Trifluoromethanesulfonyloxy-1,2,3,4-tetrahydro-naphthalene-2-carboxylic Acid (1S)-1-Methylheptyl EsterHCID 20632179—

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06703082B1
出典データセットuspto-grants-2004_03
ORD IDord-7f374d178bd64287acc3ecbfc2555bf1
出典メモuspto-grants-2004_03