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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380684Generated: October 25, 2026

Homophthalic anhydride → 2-carboxy-phenylacetic acid N-butyl-N-(2'-cyanobiphenyl-4-ylmethyl)-amide

https://huagongshe.com/reaction/2380684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHomophthalic anhydrideHCID 12801—
Reactant4'-Butylaminomethyl-2-cyanobiphenylHCID 15338353—
ReactantDichloromethane ether hexaneHCID 21850893—
Solvent1,4-DioxaneHCID 31275—
Product2-carboxy-phenylacetic acid N-butyl-N-(2'-cyanobiphenyl-4-ylmethyl)-amideHCID 53942425—

Reaction Steps

The starting material can be prepared, for example, as follows: A solution of 2.64 g of N-butyl-N-(2'-cyanobiphenyl-4-ylmethyl)-amine and 2.43 g of homophthalic acid anhydride in 50 ml of dioxane is heated under reflux for hour. After removal of the solvent, the residue is taken up in 100 ml of ethyl acetate and washed twice with 50 ml of water each time. After customary treatment, the organic phase yields a crude product that yields, from CH2Cl2 /ether/hexane, 2-carboxy-phenylacetic acid N-butyl-N-(2'-cyanobiphenyl-4-ylmethyl)-amide, m.p. 137°-139°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05369110
Source datasetuspto-grants-1994_11
ORD IDord-37e2e7bed79a4351a2f556e361619812
Source noteuspto-grants-1994_11