HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → N-{5-(4-Chlorophenyl)pent-1-en-4-yl}-N-ethoxymethyl-3,5-dimethylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Chloromethyl ethyl ether | HCID 18523 | — |
| Reactant | N-{5-(4-chlorophenyl)pent-1-en-4-yl}-3.5-dimethylbenzamide | HCID 19035936 | — |
| Catalyst | Benzyltributylammonium chloride | HCID 159952 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-{5-(4-Chlorophenyl)pent-1-en-4-yl}-N-ethoxymethyl-3,5-dimethylbenzamide | HCID 19035912 | — |
Reaction Steps
2.36 ml (25.2 mmol) of chloromethyl ethyl ether are added in small portions over the course of 2 hours to a vigorously stirred solution of 5.5 g (16.8 mmol) of N-{5-(4-chlorophenyl)pent-1-en-4-yl}-3.5-dimethylbenzamide and 100 mg of benzyltributylammonium chloride in 15 ml of 50% strength aqueous sodium hydroxide solution and 15 ml of dichloromethane at 0°-50°. The organic phase is taken up in dichloromethane and water, the organic phase is separated off, dried over sodium sulfate and evaporated to dryness under reduced pressure. The oily residue is purified by chromatography on silica gel with ethyl acetate/hexane (1:4) as mobile phase; TLC (ethyl acetate/hexane; 1:3): Rf =0.50;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05310743 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-37778db736f94abca25e9c91c75a5a51 |
| Source note | uspto-grants-1994_05 |