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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 512728생성일: 2026년 10월 26일

3,3,3-Trifluoropropene → Methyl 3-((3,3,3-Trifluoropropyl)Thio)Propionate

https://huagongshe.com/reaction/512728

반응식

참여 물질

역할이름HCID투입량
반응물3,3,3-TrifluoropropeneHCID 12672—
반응물Methyl 3-mercaptopropionateHCID 18050—
반응물2,2-Dimethoxy-2-phenylacetophenoneHCID 90571—
용매TolueneHCID 1140—
생성물Methyl 3-((3,3,3-Trifluoropropyl)Thio)PropionateHCID 118022288—

반응 단계

A 500 mL three-neck round bottomed flask was charged with toluene (200 mL) and cooled to <−50° C. with a dry ice/acetone bath. 3,3,3-Trifluoropropene (21.8 g, 227 mmol) was condensed into the reaction by bubbling the gas through the cooled solvent and the ice bath was removed. Methyl 3-mercaptopropionate (26.8 g, 223 mmol) and 2,2-dimethoxy-2-phenylacetophenone (2.72 g, 10.61 mmol) were added and a UVP lamp (4 watt) that was placed within 2 centimeters of the glass wall was turned on to the long wave function (366 nanometers). The reaction reached 35° C. due to heat from the lamp. After 4 hours, all of the trifluoropropene was either consumed or boiled out of the reaction. The light was turned off and the reaction stirred at room temperature overnight. After 22 hours, more trifluoropropene (3.1 g) was bubbled through the mixture at room temperature and the light was turned on for an additional 2 hours. The reaction had converted 93% so no more trifluoropropene was added. The light was turned off and the mixture concentrated on the rotovap (40° C., 20 torr) giving a yellow liquid (45.7 g, 21.3:1 linear:branched isomer, 75 wt % pure linear isomer determined by a GC internal standard assay, 34.3 g active, 71% in pot yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09102654B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-adabfd024de3458c833fd7cad0d84ed2
출처 메모uspto-grants-2015_08