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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638360Generated: October 30, 2026

Phenylacetic Acid → Benzeneacetamide

https://huagongshe.com/reaction/638360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetic AcidHCID 999—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
SolventDichloromethaneHCID 6344—
ProductBenzeneacetamideHCID 7680—

Reaction Steps

Using the method of Example 6, a solution of 2.81 g of phenylacetic acid in 200 ml of methylene chloride is treated at 0° C. with 3.35 g of carbonyldiimidazole. The mixture is stirred for 40 minutes. Then 2.86 g (0.0159 mole) of the (±)-amine from Example 1, Part C, above is added. The mixture is stirred for 24 hr and partitioned with saturated aqueous sodium bicarbonate. The organic phase is dried and concentrated to yield the titled (±)-benzeneacetamide product free base which is dissolved in a minimum volume of methanol and treated with one equivalent of maleic acid which has been dissolved in a minimum volume of methanol, and the mixture is diluted with diethyl ether to give the titled maleate salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04560767
Source datasetuspto-grants-1985_12
ORD IDord-4a503b511c2f4daa86b9085aab81cfbc
Source noteuspto-grants-1985_12