HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Chloro-N-(4-tert-butylphenylmethyl)-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-tert-Butylbenzylamine | HCID 2735655 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-N-(4-tert-butylphenylmethyl)-acetamide | HCID 46837194 | — |
Reaction Steps
To a suspension of commercially available 4-tert-butylbenzylamine (8.16 g, 50 mmol) and potassium carbonate (7.95 g, 57.5 mmol) in dichloromethane (100 ml) was added drop wise a solution of 2-chloroacetyl chloride (6.21 g, 55 mmol) in dichloromethane (25 ml) at room temperature. After stirring the reaction mixture at room temperature for 30 min, the reaction mixture was refluxed for 4 h. The reaction mixture was cooled and water (100 ml) was added. The phases were separated and the organic phase was dried over MgSO4 and evaporated in vacuo. The title compound was obtained as a white crystalline material which was used in the next step without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08273874B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-3c81367c8c694293baceac7f7ef0f5aa |
| Source note | uspto-grants-2012_09 |