反応 #435076
ord-fc35f6e8d1054225a1e12ff2dd7ae28b
反応方程式
cis-1-[2-[4-(6-methoxy-2-phenyl-1,2,3,4 tetrahydronaphthalen-1-yl)phenoxy]ethyl}pyrrolidine
HBr
→
cis-6-phenyl-5-[4-(2-pyrrolidin-1-ylethoxy)phenyl]-5,6,7,8-tetrahydronaphthalene-2-ol
試薬
なし
反応条件
温度
100°CELSIUS
詳細条件
See reaction.notes.procedure_details.
後処理
- 1温度The solution was cooled
- 2ろ過the resulting white precipitate was collected by filtration
- 3workup.DISSOLUTIONThe hydrobromide salt (9.6 g, 69%) was dissolved in CHCl3/MeOH
- 4その他The layers were separated
- 5抽出the aqueous layer was further extracted with CHCl3/MeOH
- 6乾燥The combined organic layers were dried (MgSO4)
- 7ろ過filtered
- 8濃縮concentrated
- 9その他to yield product as an off-white foam
実験手順
A mixture of cis-1-[2-[4-(6-methoxy-2-phenyl-1,2,3,4 tetrahydronaphthalen-1-yl)phenoxy]ethyl}pyrrolidine (12 g, 28 mmol), acetic acid (75 mL), and 48% HBr (75 mL) was heated at 100° C. for 15 h. The solution was cooled and the resulting white precipitate was collected by filtration. The hydrobromide salt (9.6 g, 69%) was dissolved in CHCl3/MeOH and was stirred with saturated NaHCO3 (aq). The layers were separated and the aqueous layer was further extracted with CHCl3/MeOH. The combined organic layers were dried (MgSO4), filtered, and concentrated to yield product as an off-white foam.