反应 #1596945
ord-609d76306b6f4c51aa02b2d46b205656
反应方程式
2-(4-benzyloxy-3-fluorophenyl)-4-bromo-5-propyltetrahydropyran
triethylamine
→
2-fluoro-4-(5-propyltetrahydropyran-2-yl)phenol
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1其他the organic phase is separated off
- 2萃取The aqueous phase is extracted with MTBE
- 3洗涤The combined organic phases are washed with water
- 4其他dried
- 5浓缩The solution is concentrated to dryness
- 6其他the residue is used directly for the following reaction
实验过程
123.0 g (0.30 mol) of 2-(4-benzyloxy-3-fluorophenyl)-4-bromo-5-propyltetrahydropyran are hydrogenated in toluene/water in the presence of Pd/C (5% of Pd) and 86.0 ml (0.60 mol) of triethylamine. The reaction solution is diluted with MTBE, and the organic phase is separated off. The aqueous phase is extracted with MTBE. The combined organic phases are washed with water and dried using sodium sulfate. The solution is concentrated to dryness, and the residue is used directly for the following reaction.