Hydrochloric Acid → Tetrahydropyranyl bromomethyl-cyclohexyl ether
反応式
[Br:1][CH2:2][CH:3]1[CH2:8][CH2:7][CH:6](O)[CH2:5][CH2:4]1.[O:10]1[CH:15]=[CH:14][CH2:13][CH2:12][CH2:11]1.Cl.C(=O)([O-])[O-:18].[K+].[K+]>>[Br:1][CH2:2][C:3]1([O:18][CH:15]2[CH2:14][CH2:13][CH2:12][CH2:11][O:10]2)[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1参加物
5
実験手順
4-Bromomethylcyclohexanol (C-5) (3.0 g) and dihydropyran (2.6 g) were mixed together and cooled with ice. A tiny drop of 10% hydrochloric acid was added. Exothermic reaction occurred and stirred at ambient temperature overnight. The solution was neutralized with potassium carbonate and extracted with dichloromethane (50 ml). It was filtered and then dichloromethane from the filtrate was evaporated to yield the compound C-6, tetrahydropyranyl bromomethyl-cyclohexyl ether (5.0 g).
後処理
- temperaturecooled with ice
- customExothermic reaction
- extractionextracted with dichloromethane (50 ml)
- filtrationIt was filtered
- customdichloromethane from the filtrate was evaporated
出典と根拠
- ORDレコード
- ord-8e0dbd93b09048068e94346ed1706d6b
- 出典データセット
- uspto-grants-1998_05
- 特許番号
- US05750300
反応ノート
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