反応式
[CH3:1][C@H:2]([O:9][C:10]([CH:12]1[CH2:21][CH2:20][C:19]2[C:14](=[CH:15][CH:16]=[C:17]([OH:22])[CH:18]=2)[CH2:13]1)=[O:11])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].C1(N[S:30]([C:33]([F:36])([F:35])[F:34])(=[O:32])=[O:31])C=CC=CC=1>ClCCl.C(N(CC)CC)C>[CH3:1][C@H:2]([O:9][C:10]([CH:12]1[CH2:21][CH2:20][C:19]2[C:14](=[CH:15][CH:16]=[C:17]([O:22][S:30]([C:33]([F:36])([F:35])[F:34])(=[O:32])=[O:31])[CH:18]=2)[CH2:13]1)=[O:11])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]参加物
5
反応物 2
生成物 1
試薬・触媒・溶媒 2
実験手順
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%).
後処理
- customquenched with water
- extractionextracted with ethyl acetate:hexane(1:1)
- washwashed with brine
- dry with materialdried over MgSO4
- concentrationconcentrated in vacuo
- customPurification by chromatography on silica gel (5% EtOAc/hexanes)
出典と根拠
- ORDレコード
- ord-7f374d178bd64287acc3ecbfc2555bf1
- 出典データセット
- uspto-grants-2004_03
- 特許番号
- US06703082B1
関連ノート
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