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p-Toluenesulfonic acid → 1-Methyl-1,3,4,9-tetrahydro-6-(phenylmethoxy)pyrano[3,4-b]indole-1-aceticacid, ethyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | Ethyl Acetoacetate | HCID 8868 | — |
| 反応物 | 5-Benzyloxy-3-(2-hydroxyethyl)indole | HCID 744849 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | 1-Methyl-1,3,4,9-tetrahydro-6-(phenylmethoxy)pyrano[3,4-b]indole-1-aceticacid, ethyl ester | HCID 131718029 | 85.3% |
反応手順
A mixture consisting of 5-benzyloxytryptophol (4.5 g, 0.017 mol), benzene (200 mL), ethyl acetoacetate (3.4 g, 0.026 mol) and p-toluenesulfonic acid (0.5 g) is refluxed for 2.5 hours using a Dean-stock trap to remove the water. The reaction mixture is cooled to room temperature and washed with 5% sodium bicarbonate, (1×200 mL), water (200 mL) and brine (100 mL), dried (MgSO4), filtered and concentrated to give 8.0 g of crude product as a thick oil, which is flash chromatographed on silica gel using 20% ethyl acetate/hexane as an eluent to afford 5.5 g oil which solidifies upon standing, m.p. 96°-98° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05229516 |
| 出典データセット | uspto-grants-1993_07 |
| ORD ID | ord-81281567c4c44990919e4c9f2a565b1f |
| 出典メモ | uspto-grants-1993_07 |