Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1265959Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1265959

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPyridineHCID 1049—
Edukttert-ButanolHCID 6386—
EduktOxalyl chlorideHCID 65578—
Edukt2-(Trifluoromethyl)acrylic acidHCID 587694—
LösungsmittelDichloromethaneHCID 6344—
Produkttert-Butyl 2-(trifluoromethyl)acrylateHCID 278228270%

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06548219B2
Quelldatensatzuspto-grants-2003_04
ORD IDord-52eda6fffece481ebb5dbc3b361f714e
Quellennotizuspto-grants-2003_04