N-Fluorobenzenesulfonimide → HCID 22175082、化合物
反応式
[CH3:1][Si:2]([CH3:15])([CH3:14])[CH2:3][CH2:4][O:5][CH2:6][O:7][C:8]1[CH:9]=[N:10][CH:11]=[CH:12][CH:13]=1.[Li]C(C)(C)C.C1C=CC(S(N(S(C2C=CC=CC=2)(=O)=O)[F:31])(=O)=O)=CC=1.CCCCCC.CC(C)=O>CCOCC.C1COCC1>[F:31][C:13]1[CH:12]=[CH:11][N:10]=[CH:9][C:8]=1[O:7][CH2:6][O:5][CH2:4][CH2:3][Si:2]([CH3:15])([CH3:14])[CH3:1]参加物
実験手順
To a stirred solution of 9 (12.39 g, 0.055 mol) in ether (200 mL) cooled to ≦−70° C. under an atmosphere of argon was slowly added t-BuLi (40 mL, 1.5 M pentane solution). During the addition, the reaction temperature was maintained at ≦−68° C. After the addition was complete the mixture was stirred an additional 60 minutes at ≦−70° C., then transferred via cannula to a stirred solution of N-fluorobenzenesulfonimide (18.92 g) in dry THF (200 mL) which was also cooled to ≦−70° C. under argon. After the addition was complete, the cooling bath was removed and the reaction mixture was allowed to warm up to room temperature. Water (100 mL) was added and the organic phase was separated, dried (MgSO4) and concentrated to give a brown oil. Chromatography (silica gel, hexane-acetone, 9:1) gave the desired product 10 as an orange oil (7.5 g) which contained about 15% starting material. This crude mixture was used directly in the next reaction.
後処理
- additionDuring the addition
- temperaturethe reaction temperature was maintained at ≦−68° C
- additionAfter the addition
- temperaturewas also cooled to ≦−70° C. under argon
- additionAfter the addition
- customthe cooling bath was removed
- additionWater (100 mL) was added
- customthe organic phase was separated
- dry with materialdried (MgSO4)
- concentrationconcentrated
- customto give a brown oil
出典と根拠
- ORDレコード
- ord-0602a33a4fa746b5b5ffb74b78f7b7f3
- 出典データセット
- uspto-grants-2006_04
- 特許番号
- US07034035B2
反応ノート
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