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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520834Generated: October 30, 2026

Triethylamine → Methyl 5-bromo-2-(2-(4-cyanophenoxy)acetamido)benzoate

https://huagongshe.com/reaction/520834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl 2-amino-5-bromobenzoateHCID 736224—
ReactantAcetyl chloride, (4-cyanophenoxy)-HCID 12207748—
SolventDichloromethaneHCID 6344—
ProductMethyl 5-bromo-2-(2-(4-cyanophenoxy)acetamido)benzoateHCID 8112554—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methyl 2-amino-5-bromobenzoate (4.0 g, 17.39 mmol) in dichloromethane (60 mL) was added 2-(4-cyanophenoxy)acetyl chloride (3.74 g, 19.13 mmol, Intermediate 2: step a) to form a thick suspension. An additional 30 mL of dichloromethane was added. The reaction was then cooled to 0° C. and triethylamine (5.32 mL, 38.25 mmol) was added dropwise. The cold bath was removed and the reaction was stirred at room temperature for 2 hours, then filtered to give the title compound as a white solid. The filtrate was washed with water, followed by saturated aqueous NH4Cl solution. The organic layer was dried (MgSO4), filtered, concentrated, and the residue was purified by flash column chromatography (silica gel, 20% EtOAc-heptane) to afford more of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328095B2
Source datasetuspto-grants-2016_05
ORD IDord-3a118594e5f545bab24dbba9266820d9
Source noteuspto-grants-2016_05