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HRID 57109Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/57109

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,3,3-TrifluoropropeneHCID 12672—
EduktMethyl 3-mercaptopropionateHCID 18050—
Edukt2,2-Dimethoxy-2-phenylacetophenoneHCID 90571—
LösungsmittelTolueneHCID 1140—
ProduktMethyl 3-((3,3,3-Trifluoropropyl)Thio)PropionateHCID 118022288—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434712B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-f0413aa408994cf3967fdad595315297
Quellennotizuspto-grants-2016_09