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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantPivalic acidHCID 6417—
ReactantTriethylamineHCID 8471—
ReactantHOAtHCID 181649—
Reactant4-AminobenzylamineHCID 427814—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-(4-aminobenzyl)pivalamideHCID 1867251483.4%

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403612B2
Source datasetuspto-grants-2002_06
ORD IDord-d6837e735f1543fab1c0e1eb248b5700
Source noteuspto-grants-2002_06