化工社化工社 化学情報印刷レポート · 研究参考用
Hydrochloric Acid → 6,7-Dimethoxy-1-methyl-1,2,3,4-tetrahydroisoquinoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 反応物 | 6,7-Dimethoxy-1-methyl-3,4-dihydroisoquinoline hydrochloride | HCID 12327303 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 6,7-Dimethoxy-1-methyl-1,2,3,4-tetrahydroisoquinoline | HCID 10302 | 100% |
反応手順
To a stirred solution of 3,4-dihydro-6,7-dimethoxy-1-methylisoquinoline hydrochloride (47.0 g, 0.229 m) and NaOH (5 g) in absolute methanol (500 ml) was added NaBH4 (34.6 g, 0.917 m) and the mixture stirred for 2 hr (TLC complete) and allowed to stand overnight. The mixture was cooled in an ice bath, treated carefully with 20% HCl until pH 1 was achieved and then heated to 50° for 1 hr. The solvent was then removed on the aspirator and the residue dissolved in 1 liter H2O. The solution was basified to pH 11 with NaOH (20%) and extracted with 3×250 ml CHCl3. The extracts were dried over MgSO4 and evaporated to give 1,2,3,4-tetrahydro-6,7-dimethoxy-1-methylisoquinoline as an oil, 47.6 g (100% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04766131 |
| 出典データセット | uspto-grants-1988_08 |
| ORD ID | ord-53a5cec0dbdf4e6f814abe1d111d366b |
| 出典メモ | uspto-grants-1988_08 |