反応式
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[O:10][CH3:11])[CH2:5][OH:6].CC([O-])(C)C.[K+].[CH2:18](Cl)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>C(O)CC>[CH2:18]([O:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[O:10][CH3:11])[CH2:5][OH:6])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1参加物
実験手順
A solution of 3-hydroxy-4-methoxy-benzyl alcohol (61.67 g, 400 mmole) in 1-propanol (600 ml) was treated at 60° C. with 97% t-BuOK (55.52 g, 480 mmole), at 90° C. with benzyl chloride (66.57 ml, 560 mmole) and the resulting mixture heated under reflux for 2 hours. Then at 90° C. a second batch of t-BuOK (9.25 g, 80 mmole) was added. After a further hour at reflux a third batch of t-BuOK (9.25 g, 80 mmol) and a second batch of benzyl chloride (9.51 ml, 80 mmole) was added at 90° C. After a further 2.5 hours at reflux the mixture was cooled to room temperature and the solid filtered off. The solvents were removed in vacuo, the residue treated with water (300 ml) and one-third of the solvent removed in vacuo. Water (100 ml) was added to the residue, which was then distilled off in vacuo and the procedure repeated. The resulting suspension was filtered, the solid was collected, dried and triturated with petroleum ether (2×600 ml) to give 3-benzyloxy-4-methoxy-benzyl alcohol, (86.21 g, 88.2%) mp 62-65° C.
後処理
- temperaturethe resulting mixture heated
- temperatureunder reflux for 2 hours
- temperatureAfter a further 2.5 hours at reflux the mixture
- filtrationthe solid filtered off
- customThe solvents were removed in vacuo
- additionthe residue treated with water (300 ml) and one-third of the solvent
- customremoved in vacuo
- additionWater (100 ml) was added to the residue, which
- distillationwas then distilled off in vacuo
- filtrationThe resulting suspension was filtered
- customthe solid was collected
- customdried
- customtriturated with petroleum ether (2×600 ml)
出典と根拠
- ORDレコード
- ord-3dcb48659071488e86420061ef5104b4
- 出典データセット
- uspto-grants-2001_05
- 特許番号
- US06228859B1
関連ノート
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