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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397958Generated: October 27, 2026

Oxalyl chloride → 4,4,4-Trifluorobutanoyl chloride

https://huagongshe.com/reaction/397958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant4,4,4-Trifluorobutanoic acidHCID 2777085—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product4,4,4-Trifluorobutanoyl chlorideHCID 1510447457%

Reaction Steps

Method 5 General Experimental: 4,4,4-Trifluorobutyric acid (70.0 mmol, 10.0 g) in CH2Cl2 (190 ml) was treated with oxalyl chloride (140 mmol, 12.3 ml) and DMF (1 drop), then heated to reflux for 1 h. Solvent and excess oxalyl chloride were removed from the volatile product by simple distillation of the reaction mixture at atmospheric pressure to provide crude 4,4,4-trifluorobutyric acid chloride (6.4 g). 1H NMR (CDCl3) δ3.20 (2H, t, J=7.2), 2.65-2.45 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610730B2
Source datasetuspto-grants-2003_08
ORD IDord-3457df89a6ff4cc682b368a4d2df3080
Source noteuspto-grants-2003_08