돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1199860생성일: 2026년 10월 27일

Dichloromethane → 3-Chloro-4-phenylthio-1,1,2-trifluoro-1-butene

https://huagongshe.com/reaction/1199860

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Alkenes, C4-20 alpha-, gamma-omega-perfluoroHCID 109645—
반응물Benzenesulfenyl chlorideHCID 11008040—
촉매Calcium CarbonateHCID 10112—
생성물3-Chloro-4-phenylthio-1,1,2-trifluoro-1-buteneHCID 1404344997.5%

반응 단계

To a solution of 1,1,2-trifluoro-1,3-butadiene (8.0 g. 74 mmol) and calcium carbonate (50 mg) in 85 mL of dichloromethane at -40° C. in a round-bottom 250 mL flask was added a solution of phenylsulfenyl chloride (7.1 g, 49 mmol) in 20 mL of dichloromethane over 2 hours. The reaction mixture was left to stand overnight at room temperature and poured into ice water. The organic layer was washed with aqueous 5% sodium metabisulfite solution and brine, then dried over anhydrous magnesium sulfate. Evaporation of solvent followed by distillation gave 12.1 g (97.5%) of 3-chloro-4-phenylthio-1,1,2-trifluoro-1-butene as a light yellow oil, bp 84°-86° C. (1.0 mm Hg). 1H-NMR (300 MHz, CDCl3): δ 3.39(2H, d, J=8 Hz), 4.58(1H, ttd, J=1.5, 8, 33 Hz), 7.2-7.4(5H, phenyl protons). Mass spectrum: m/e=252,254 (M+). 19F-NMR (300 MHz, CDCl3): φ F3 =-11.8, F2 =116.7, F1 =99.3. J(F12 =64.5, J(F23)=111.2, J(F13)=33.0, J(F3H)=26.4.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04902835
출처 데이터셋uspto-grants-1990_02
ORD IDord-abfc180c428e46f59b74498849c432e8
출처 메모uspto-grants-1990_02