Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128824Generated: October 26, 2026

3-Methylsulfanyl-5-trifluoromethyl-1,3-dihydro-indol-2-one → 5-(Trifluoromethyl)oxindole

https://huagongshe.com/reaction/128824

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methylsulfanyl-5-trifluoromethyl-1,3-dihydro-indol-2-oneHCID 12351491—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Product5-(Trifluoromethyl)oxindoleHCID 373445790%

Reaction Steps

A solution of 3-(methylthio)-5-(trifluoromethyl)oxindole (Gassman P. G., Cue B. W., Luh T-Y, J. Org. Chem. 1977;42:1344-1348) (10 g, 40 mmol) in AcOH (100 mL) was heated under reflux with Zn dust (13.3 g, 0.2 mol) for 1 hour. The mixture was cooled and filtered, and the precipitate was washed with AcOH. The combined filtrates were evaporated under reduced pressure, and the residue was diluted with 1M aqueous ammonia to give 5-trifluoromethyloxindole [VII: R1 =5-CF3, R3 =H] (7.22 g, 90%); mp (aqueous EtOH) 188.5°-191° C. (lit. [Hardtmann G. E., U.S. Pat. No. 4,160,032; Chem. Abstr, 1979;91:P107890w]; mp 188°-189° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05464861
Source datasetuspto-grants-1995_11
ORD IDord-a466cc9e1e6d44b283c7b6fa96093cea
Source noteuspto-grants-1995_11