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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627464Generated: October 30, 2026

Phenylacetyl chloride → Methyl 5-bromo-2-(2-phenylacetamido)benzoate

https://huagongshe.com/reaction/627464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyl chlorideHCID 7679—
ReactantTriethylamineHCID 8471—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-amino-5-bromobenzoateHCID 736224—
SolventDichloromethaneHCID 6344—
ProductMethyl 5-bromo-2-(2-phenylacetamido)benzoateHCID 19168685—

Reaction Steps

To a mixture of methyl 2-amino-5-bromobenzoate (9.00 g, 39.1 mmol) and Et3N (7.6 mL, 54.8 mmol) in CH2Cl2 (90 mL) was added 2-phenylacetyl chloride (7.26 g, 46.9 mmol) at 4° C. dropwise. After completion of the addition, the cooling bath was removed and the mixture was stirred for 27 hours. TLC showed some of the starting material methyl 2-amino-5-bromobenzoate still remained. More 2-phenylacetyl chloride (1.88 g, 12.2 mmol) and Et3N (2.2 mL, 15.9 mmol) were added, and the mixture was stirred overnight. K2CO3 (aqueous) was added, the organic layer was separated, and the aqueous layer was extracted with CH2Cl2. The combined organic layers were washed with water, dried (Na2SO4), filtered, and concentrated in vacuo. CH3CN (100 mL) was added, and the precipitated solid was filtered, washed with Et2O, and dried to give the title compound. The filtrate was concentrated in vacuo, and the solid was filtered, washed with Et2O, and dried to give more title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309222B2
Source datasetuspto-grants-2016_04
ORD IDord-22bfb6df96e14543881847cd7113bd89
Source noteuspto-grants-2016_04