HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethylamine → N,N-diethyl-2-tert-butylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | tert-Butylbenzoic acid (mixed isomers) | HCID 136850 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N,N-diethyl-2-tert-butylbenzamide | HCID 18630191 | — |
Reaction Steps
A solution of 2-tert-butylbenzoic acid (4.0 g, 22.5 mmol) in thionyl chloride (8.2 mL, 112 mmol) was stirred at RT for 2 h, then was concentrated three times from carbon tetrachloride to remove all traces of excess thionyl chloride. A solution of diethylamine (4.93 g, 67.4 mmol) in CH2Cl2 (10 mL) was added dropwise over 10 min to an ice water-cooled solution of the crude acid chloride in CH2Cl2 (35 mL). Ten min after addition was complete, the reaction was partitioned between ether and 10% HCl. The ether phase was then washed with sat aq NaHCO3, then was dried (MgSO4), and concentrated to afford a quantitative yield of N,N-diethyl-2-tert-butylbenzamide as an off-white solid. m.p. 38.5°-40.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05705513 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-71a2ad744c9547d592994ec6d5059218 |
| Source note | uspto-grants-1998_01 |