関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4'-Hydroxyacetophenone | HCID 7469 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 3-(Diethylamino)-1-propanol | HCID 12159 | — |
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | Methanesulfonate | HCID 85257 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 1-(4-[3-(Diethylamino)propoxy]phenyl)ethanone | HCID 11858361 | — |
反応手順
To a stirred solution of 4′-hydroxyacetophenone (91 mmol) in DMF (80 mL) at rt, solid potassium carbonate (153 mmol) was added. The mesylate prepared from 3-diethylamino-1-propanol and methanesulfonyl chloride (76 mmol) was added to the reaction mixture and heated to 80° C. until completion according to General Procedure Q1, as indicated by TLC or HPLC. After cooling to rt, the reaction mixture was quenched by treating the mixture with saturated sodium bicarbonate. The aqueous layer was poured into EtOAc (100 mL) and washed with H2O (2×50 mL) and brine (50 mL). The organic layer was dried over sodium sulfate, and the solvent was removed in vacuuo to afford the desired 1-{4-[3-(diethylamino)propoxy]phenyl}ethanone. The crude alkylated product was used for further transformation after purifying using silica gel column chromatography (1-4% MeOH/DCM).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07737285B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-8310e01060ad4b869e476204a2d27343 |
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| 出典メモ | uspto-grants-2010_06 |
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