Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190366Generated: October 29, 2026

Oxalyl chloride → 3-(1-Cyanocyclopropyl)benzoyl chloride

https://huagongshe.com/reaction/2190366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant3-(1-Cyanocyclopropyl)benzoic acidHCID 57441039—
CatalystDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product3-(1-Cyanocyclopropyl)benzoyl chlorideHCID 86631982—

Reaction Steps

To a solution of 3-(1-cyanocyclopropyl)benzoic acid (10.0 g, 53.4 mmol) produced in Example A1(iii) in tetrahydrofuran (130 mL) were added oxalyl chloride (5.47 mL, 64.1 mmol) and N,N-dimethylformamide (2 drops), and the mixture was stirred at room temperature for 3 hr. The reaction mixture was concentrated under reduced pressure to give 3-(1-cyanocyclopropyl)benzoyl chloride as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324395B2
Source datasetuspto-grants-2012_12
ORD IDord-b31fa846190d455aabe744e1e42f6f43
Source noteuspto-grants-2012_12