反応式
[Br-].[C:2]([C:6]1[CH:31]=[CH:30][C:9]([CH2:10][P+](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=[CH:8][CH:7]=1)([O:4][CH3:5])=[O:3].[CH:32]([C:34]1[CH:43]=[CH:42][C:37]([C:38]([O:40][CH3:41])=[O:39])=[CH:36][CH:35]=1)=O.C1(C)C=CC=CC=1.C[O-].[Na+]>CO>[C:38]([C:37]1[CH:42]=[CH:43][C:34]([CH:32]=[CH:10][C:9]2[CH:8]=[CH:7][C:6]([C:2]([O:4][CH3:5])=[O:3])=[CH:31][CH:30]=2)=[CH:35][CH:36]=1)([O:40][CH3:41])=[O:39]参加物
実験手順
To a 1 L 3-neck round bottom flask fitted with a glass stopper, rubber septum, and reflux condenser fitted with a nitrogen inlet tube, was added 20.0 g (39.77 mmol) (4-carbomethoxy) benzyltriphenylphosphonium bromide; 7.83 g (47.73 mmol) methyl 4-formylbenzoate; and 110 mL 2:1 methanol: toluene. After the starting material dissolved, 10.0 mL (43.75 mmol) 25% sodium methoxide solution in methanol was added dropwise over several minutes. The reaction vessel was heated at reflux for 30 minutes. After cooling to room temperature, the reaction vessel was cooled at 0° C. for several hours. The resulting precipitate was filtered, washed with 2:1 methanol: toluene, and dried in a vacuum oven to afford 5.54 g (72%) of the compound as a 57:43 mixture of cis: trans isomers.
後処理
- customTo a 1 L 3-neck round bottom flask fitted with a glass stopper, rubber septum
- temperaturereflux condenser
- customfitted with a nitrogen inlet tube
- dissolutionAfter the starting material dissolved
- temperatureThe reaction vessel was heated
- temperatureat reflux for 30 minutes
- temperaturethe reaction vessel was cooled at 0° C. for several hours
- filtrationThe resulting precipitate was filtered
- washwashed with 2:1 methanol
- dry with materialtoluene, and dried in a vacuum oven
出典と根拠
- ORDレコード
- ord-cdafc08746c54bb2b0d1586fd2da73e7
- 出典データセット
- uspto-grants-1992_11
- 特許番号
- US05164100
関連ノート
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