HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185957Generated: October 27, 2026
1,2-Dichloroethane → N-(4-aminobenzyl)pivalamide
https://huagongshe.com/reaction/2185957
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Pivalic acid | HCID 6417 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | 4-Aminobenzylamine | HCID 427814 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(4-aminobenzyl)pivalamide | HCID 18672514 | 83.4% |
Reaction Steps
To a solution of trimethyl acetic acid (9.98 g, 97.7 mmol) in methylene chloride (200 ml) cooled to 0° C. is added 4-aminobenzyl amine (11.1 ml, 97.7 mmol), triethyl amine (34.1 ml, 244 mmol), HOAt (13.3 g, 97.7 mmol), and EDC (18.73 g, 97.7 mmol). The reaction mixture is allowed to slowly warm to 25° C. and stirred at this temperature for 18 hrs. The reaction mixture is diluted with water and the organic layer is extracted, washed with aqueous sodium bicarbonate and brine, dried over magnesium sulfate and concentrated in vacuo. The crude product is purified by flash chromatography (silica gel, 40% to 65% ethyl acetate in hexane) to give N-(4-amino-benzyl)-2,2-dimethyl-propionamide (16.8 g), as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06403612B2 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-d6837e735f1543fab1c0e1eb248b5700 |
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| Source note | uspto-grants-2002_06 |
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