반응식
[CH3:1][C:2]([C:4]1[C:9](O)=[CH:8][C:7](O)=[CH:6][C:5]=1O)=[O:3].C(Cl)C1C=CC=CC=1.C([O-])([O-])=O.[K+].[K+]>CN(C=O)C.[Na+].[Cl-]>[C:2]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)(=[O:3])[CH3:1]참가 물질
6
실험 절차
To a solution of 1.68g of phloroacetophenone and 12.7 g of benzyl chloride in 20 ml of DMF is added 5.53 g of anhydrous K2CO3. The mixture is stirred for 16 hours at 65° under argon. The mixture is diluted with 100 ml of 5% NaCl and extracted with ethyl acetate (2 × 50 ml). The extracts are washed with 5% NaCl and 2% NaOH, dried over MgSO4 and concentrated to a red oil which is purified on a dry 250 g silica gel columning CCl4 as eluent. This yields 2,4,6-tribenzyloxyacetophenone as a yellow oil.
후처리
- extractionextracted with ethyl acetate (2 × 50 ml)
- washThe extracts are washed with 5% NaCl and 2% NaOH
- dry with materialdried over MgSO4
- concentrationconcentrated to a red oil which
- customis purified on a dry 250 g silica gel
출처 및 근거
- ORD 기록
- ord-37b556da94d4454a8425a0e130f35973
- 출처 데이터셋
- uspto-grants-1977_03
- 특허 번호
- US04013801
연결된 노트
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