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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762174Generated: October 26, 2026

4-tert-Butylbenzoic acid → Methyl 4-[2-(4-tert-butylbenzamido)ethoxy]benzoate

https://huagongshe.com/reaction/1762174

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-Butylbenzoic acidHCID 7403—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantMethyl 4-(2-aminoethoxy)benzoateHCID 14097616—
SolventChloroformHCID 6212—
ProductMethyl 4-[2-(4-tert-butylbenzamido)ethoxy]benzoateHCID 1442662591.9%

Reaction Steps

p-tert-Butylbenzoic acid (5.35 g) and 3.34 g of triethylamine were dissolved in 70 ml of chloroform and 3.26 g of ethyl chloroformate was dropped into the above mixture with stirring and cooling at 0° to 5° C. After the dropping, the mixture was stirred at the same temperature for 30 minutes and, after addition of 5.86 g of methyl 4-(2-aminoethoxy)benzoate thereto, the mixture was stirred for 6 hours more. The reaction solution was washed with 10% hydrochloric acid, saturated potassium carbonate solution, and water, dried with anhydrous magnesium sulpahte, concentrated in vacuo, and the residue was crystallised with n-hexane to give 9.8 g of crystals which were further recrystallised from ethyl acetate to give 7.64 g (yield: 71.65%) of the product, m.p. 112°-114° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04831055
Source datasetuspto-grants-1989_05
ORD IDord-7c50a48fc6d84b4197668e9e297aa4e0
Source noteuspto-grants-1989_05