2-Phenylethyl Acetate → 4-(5-Bromo-2-chlorobenzoyl)phenethyl acetate
反応式
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([Cl:11])=[C:6]([CH:10]=1)[C:7]([OH:9])=O.C(Cl)(=O)C(Cl)=O.[Cl-].[Cl-].[Cl-].[Al+3].[C:22]([O:25][CH2:26][CH2:27][C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)(=[O:24])[CH3:23]>C(Cl)Cl.CN(C=O)C>[C:22]([O:25][CH2:26][CH2:27][C:28]1[CH:33]=[CH:32][C:31]([C:7](=[O:9])[C:6]2[CH:10]=[C:2]([Br:1])[CH:3]=[CH:4][C:5]=2[Cl:11])=[CH:30][CH:29]=1)(=[O:24])[CH3:23]参加物
実験手順
To a solution of commercially available 5-bromo-2-chlorobenzoic acid (5 g, 21.23 mmol) in 30 mL of anhydrous DCM was added a catalytic amount of DMF followed by oxalyl chloride (1.95 mL, 22.3 mmol) and stirred for 2 h at room temperature. A mixture of aluminum trichloride (3.68 g, 27.6 mmol) and phenethyl acetate (3.38 mL, 21.23 mmol) in 15 mL DCM was cooled in an ice-bath and the acid chloride was transferred to it using a canula. The mixture was stirred at room temperature for 4 h. The mixture was poured into 100 mL of ice-cold water and the organic layer was isolated. The aqueous solution was extracted with 25 mL DCM. The combined organic solution was washed with brine (25 mL) and dried (Na2SO4), filtered and evaporated. Purification on silica gel using an ISCO column with 5:1 hexane:EtOAc followed by 10:1 hexane:EtOAc gave intermediate BF (2.1 g, yield 26%). 1H NMR (300 MHz, CDCl3): δ 8.12 (d, J=2.4 Hz, 1H), 7.71 (d, J=8.4 Hz, 1H), 7.59 (d, J=2.7 Hz, 1H), 7.56 (d, J=8.4 Hz, 1H), 7.36 (s, 1H), 7.33 (d, J=8.4 Hz, 1H), 7.30 (d, J=8.4 Hz, 1H), 4.31 (t, J=6.9, 6.6 Hz, 2H), 3.01 (t, J=6.9, 6.6 Hz, 2H), 2.04 (s, 3H).
後処理
- temperaturewas cooled in an ice-bath
- stirringThe mixture was stirred at room temperature for 4 h
- customthe organic layer was isolated
- extractionThe aqueous solution was extracted with 25 mL DCM
- washThe combined organic solution was washed with brine (25 mL)
- dry with materialdried (Na2SO4)
- filtrationfiltered
- customevaporated
- customPurification on silica gel using an ISCO column with 5:1 hexane
- customEtOAc gave intermediate BF (2.1 g, yield 26%)
出典と根拠
- ORDレコード
- ord-9ace20d09e36429da144d73d2a957246
- 出典データセット
- uspto-grants-2012_01
- 特許番号
- US08106021B2
反応ノート
読み込み中…