HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → 3-(chloromethyl)-N,N-dimethylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(Chloromethyl)benzoyl chloride | HCID 2733324 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(chloromethyl)-N,N-dimethylbenzamide | HCID 21874604 | 71.2% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A solution of dimethylamine (2.91 mL, 5.82 mmol, 2.0M THF), NEt3 (0.885 mL, 6.35 mmol) and CH2Cl2 30 mL was cooled to 0° C. 3-(Chloromethyl)benzoyl chloride (1.0 g, 5.29 mmol) was added as a CH2Cl2 solution (3 mL) and the solution was stirred at 0° C. for 2 hours and then at ambient temperature for 2 hours. The reaction was washed with 1N HCl followed by brine, and the organic layer was dried over Na2SO4, filtered and concentrated. The product was purified by column chromatography (EtOAc) to provide 0.745 g (71%) of the product as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09174981B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-493d0501f551417882496be2877a7143 |
| Source note | uspto-grants-2015_11 |