Sodium Carbonate → 3-Benzo[1,3]dioxol-5-yl-5-benzyloxy-benzoic Acid Methyl Ester
반응식
[CH3:1][O:2][C:3](=[O:26])[C:4]1[CH:9]=[C:8](OS(C(F)(F)F)(=O)=O)[CH:7]=[C:6]([O:18][CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH:5]=1.[C:27](=[O:30])([O-])[O-:28].[Na+].[Na+]>COCCOC.O.C1OC2C=CC(B(O)O)=CC=2O1.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH3:1][O:2][C:3](=[O:26])[C:4]1[CH:5]=[C:6]([O:18][CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH:7]=[C:8]([C:4]2[CH:9]=[CH:8][C:7]3[O:28][CH2:27][O:30][C:6]=3[CH:5]=2)[CH:9]=1참가 물질
7
반응물 2
생성물 1
시약·촉매·용매 4
실험 절차
3-Benzyloxy-5-trifluoromethanesulfonyloxy-benzoic acid methyl ester (15.4 g) was dissolved in 1,2-dimethoxyethane (250 mL), followed by addition of Pd(PPh3)4 (2.5 g), solution of sodium carbonate (12 g) in water (120 mL) and 3,4-methylenedioxyphenylboronic acid (8.4 g). The resulting reaction mixture was refluxed under the flow of nitrogen for 5 h. After cooling the organic layer was separated and washed with water and then dried over magnesium sulfate. The crude material was purified on a silica gel column using ethyl acetate and hexanes to yield 14.2 g (99% yield) of the title compound.
후처리
- customThe resulting reaction mixture
- temperaturewas refluxed under the flow of nitrogen for 5 h
- temperatureAfter cooling the organic layer
- customwas separated
- washwashed with water
- dry with materialdried over magnesium sulfate
- customThe crude material was purified on a silica gel column
출처 및 근거
- ORD 기록
- ord-71719f249d7b4f4da28739d19782df74
- 출처 데이터셋
- uspto-grants-2011_08
- 특허 번호
- US07989454B2
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