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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397255Generated: October 25, 2026

Hydrochloric Acid → tert-Butyl 2-(trifluoromethyl)acrylate

https://huagongshe.com/reaction/397255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
Reactanttert-ButanolHCID 6386—
ReactantOxalyl chlorideHCID 65578—
Reactant2-(Trifluoromethyl)acrylic acidHCID 587694—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 2-(trifluoromethyl)acrylateHCID 278228270%

Reaction Steps

Oxalyl chloride (87.3 g, 0.68 mol) was added to a solution of 2-(trifluoromethyl)acrylic acid (TFMAA) (15.0 g, 0.11 mol) in methylene chloride (90 mL) in a dropwise manner at room temperature under an nitrogen atmosphere. The solution was heated to reflux for 5 hours, and the solvent and excess reagent were removed on a rotary evaporator. The resulting acid chloride was added to a stirred solution consisting of t-butanol (44 g, 0.59 mmol) and pyridine (33.6 g, 0.42 mol) in methylene chloride at 0° C. over a 10 min period. After stirring overnight at room temperature, the solution was neutralized with diluted aqueous HCl and washed with saturated aqueous sodium bicarbonate. The organic phase was removed, and the aqueous phase was extracted with pentane. The combined organic solvents were reduced to a small volume by distillation and then the residue was chromatographed on a column of silica gel. The product was re-purified by distillation to give 14.0 g of TBTFMA as a colorless liquid (70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610456B2
Source datasetuspto-grants-2003_08
ORD IDord-2a7f1f02b4d24ebbace059ba10ac2811
Source noteuspto-grants-2003_08