Hydroxylamine → 6-(4'-Chloro-biphenyl-4-ylsulfanyl)-hexanoic acid
反応式
C[O:2][C:3](=[O:23])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][S:9][C:10]1[CH:15]=[CH:14][C:13]([C:16]2[CH:21]=[CH:20][C:19]([Cl:22])=[CH:18][CH:17]=2)=[CH:12][CH:11]=1.NO.[OH-].[K+].CO>C1COCC1>[Cl:22][C:19]1[CH:20]=[CH:21][C:16]([C:13]2[CH:14]=[CH:15][C:10]([S:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][C:3]([OH:23])=[O:2])=[CH:11][CH:12]=2)=[CH:17][CH:18]=1参加物
反応条件
- 温度
- 0 °C
実験手順
To a solution of 6-(4′-chloro-biphenyl-4-ylsulfanyl)-hexanoic acid methyl ester (1.0 g, 2.9 mmol) in distilled THF (20 mL) containing 50% aqueous hydroxylamine (1.9 mL, 28.8 mmol) was added at 0° C. a solution of potassium hydroxide in methanol (5.0 mL, 1M, 5.0 mmol) in a dropwise manner. After stirring at 0° C. for 1 h, distilled water (20 mL) was added and the mixture was made neutral by dropwise addition of concentrated hydrochloric acid (10 M) at 0° C. The aqueous solution was extracted with ethyl acetate (2×40 mL) and the combined extracts were washed with brine (80 mL), dried over anhydrous MgSO4, filtered and evaporated to dryness. The residue was recrystallised from acetone to give the title compound (923 mg, 91%) as a white powder, mp 156-157° C.
後処理
- distillationdistilled water (20 mL)
- additionwas added
- additionthe mixture was made neutral by dropwise addition of concentrated hydrochloric acid (10 M) at 0° C
- extractionThe aqueous solution was extracted with ethyl acetate (2×40 mL)
- washthe combined extracts were washed with brine (80 mL)
- dry with materialdried over anhydrous MgSO4
- filtrationfiltered
- customevaporated to dryness
- customThe residue was recrystallised from acetone
出典と根拠
- ORDレコード
- ord-5dc331e3b0334694a85be06bbff59b54
- 出典データセット
- uspto-grants-2010_03
- 特許番号
- US07683185B2
反応ノート
読み込み中…