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Tetrahydrofuran → Ethyl 5-chloro-3-phenylthioindole-2-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | S-Phenyl benzenethiosulphonate | HCID 71031 | — |
| 反応物 | Ethyl 5-chloroindole-2-carboxylate | HCID 78518 | — |
| 反応物 | HCID 178418443 | HCID 178418443 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Ammonium Chloride | HCID 25517 | — |
| 生成物 | Ethyl 5-chloro-3-phenylthioindole-2-carboxylate | HCID 86745392 | — |
反応手順
To a cold (0°), stirred solution of ethyl 5-chloroindole-2-carboxylate (223 mg) in 4.5 mL dry tetrahydrofuran, under argon, was added 0.55 mL of a solution of ethylmagnesium bromide in ether. The resultant mixture was stirred for 30 min then cooled to -78°. Solid S-phenyl benzenethiosulfonate (300 mg) was added and the mixture stirred at 78° for 30 min and 0° for 1 h. The mixture was then diluted with ether and saturated aqueous ammonium chloride added. The organic layer was separated, washed with water and brine and dried over MgSO4. Filtration and concentration gave a yellow oil which was purified by flash chromatography on silica gel. Elution with hexane-ethyl acetate (85:15) gave the title product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05081138 |
| 出典データセット | uspto-grants-1992_01 |
| ORD ID | ord-e0c79a883be944ecb464d0b26ed2382a |
| 出典メモ | uspto-grants-1992_01 |