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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713730Generated: October 26, 2026

Benzoyl chloride → Methyl 4-(2-benzenecarbonylamino-ethoxy)benzoate

https://huagongshe.com/reaction/713730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantMethyl 4-(2-aminoethoxy)benzoate hydrochlorideHCID 50988568—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-(2-benzenecarbonylamino-ethoxy)benzoateHCID 14426627—

Reaction Steps

To a suspension of methyl 4-(2-amino-ethoxy)benzoate hydrochloride (0.232 g, 1 mmol) in THF (6 ml) was added benzoyl chloride (0.140 g, 1 mmol) followed by triethylamine (0.121 g, 1.2 mmol). The reaction mixture was stirred for 1 h and then diluted with ethyl acetate. The organic layer was washed with 0.5 M aqueous HCl, saturated sodium bicarbonate solution, and brine. The organic layer was concentrated in vacuo to give methyl 4-(2-benzenecarbonylamino-ethoxy)benzoate which was directly used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09186347B1
Source datasetuspto-grants-2015_11
ORD IDord-e1051e9b5aa646ac959a7f5d8b6ad80e
Source noteuspto-grants-2015_11