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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234756Generated: October 29, 2026

Triethylamine → N-(1-Hydroxy-2-methylpropan-2-yl)-2-methoxybenzamide

https://huagongshe.com/reaction/234756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Methoxybenzoic acidHCID 11370—
Reactant2-Amino-2-methyl-1-propanolHCID 11807—
ReactantHCID 178524978HCID 178524978—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-(1-Hydroxy-2-methylpropan-2-yl)-2-methoxybenzamideHCID 2764140—

Reaction Steps

15.2 g (100 mmol) of 2-methoxy-benzoic acid are dissolved in 300 ml of methylene chloride and the solution is stirred with 14.2 g (105 mmol) of 1-hydroxy-benzoic acid triazole×1 H2O and 21.66 g (105 mmol) of N,N-dicyclohexylcarbodiimide at 0° C. The suspension thus obtained is stirred at room temperature for 0.5 hour, cooled to 0° C. again, and a solution of 9.89 g (111 mmol) of 1-hydroxy-2-methyl-2-propylamine and 12.65 g (125 mmol) of triethylamine in 300 ml of methylene chloride is added. The reaction is complete after 1 hour. The reaction mixture is washed with 1M of hydrochloric acid and saturated sodium bicarbonate solution, dried over sodium sulphate and concentrated in vacuo. The crude product is stirred with petroleum ether, filtered off with suction, subsequently rinsed with the solvent and dried under a high vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05596006
Source datasetuspto-grants-1997_01
ORD IDord-f2496074f91240a19a3ec732862e7cdd
Source noteuspto-grants-1997_01