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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 900042생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/900042

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물PyridineHCID 1049—
반응물tert-ButanolHCID 6386—
반응물Oxalyl chlorideHCID 65578—
반응물2-(Trifluoromethyl)acrylic acidHCID 587694—
용매DichloromethaneHCID 6344—
생성물tert-Butyl 2-(trifluoromethyl)acrylateHCID 278228270%

반응 단계

Oxalyl chloride (87.3 g, 0.68 mol) was added to a solution of TFMAA (15.0 g, 0.11 mol) in methylene chloride (90 mL) in a dropwise manner at room temperature under a 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 dichloromethane at 0O 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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07358027B2
출처 데이터셋uspto-grants-2008_04
ORD IDord-56a48c84f9a446b79904258af54da0c5
출처 메모uspto-grants-2008_04