참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4'-Hydroxyacetophenone | HCID 7469 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 3-(Diethylamino)-1-propanol | HCID 12159 | — |
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 반응물 | Methanesulfonate | HCID 85257 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 1-(4-[3-(Diethylamino)propoxy]phenyl)ethanone | HCID 11858361 | — |
반응 단계
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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07737285B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-30834c4dd61b49dc904e22cfb6d1f1b8 |
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| 출처 메모 | uspto-grants-2010_06 |
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