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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17061Generated: October 26, 2026

Water → [3-(Methylthio)-5-(trifluoromethyl)phenyl]methanol

https://huagongshe.com/reaction/17061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTert-Butyl nitriteHCID 10906—
ReactantDimethyl DisulfideHCID 12232—
Reactant(3-Amino-5-(trifluoromethyl)phenyl)methanolHCID 53414333—
SolventChloroformHCID 6212—
Product[3-(Methylthio)-5-(trifluoromethyl)phenyl]methanolHCID 68687257—

Reaction Steps

To a solution of [3-amino-5-(trifluoromethyl)phenyl]methanol (319 mg, 1.67 mmol) (Step A, Example 24) in CHCl3 (5 mL) was added dimethyl disulfide (296 μL, 3.34 mmol). Next, t-butyl nitrite (285 μL, 2.4 mmol) was added dropwise by syringe. The reaction was stirred at room temperature for two hours and then poured into H2O (15 mL). The mixture was extracted with EtOAc (50 mL), washed with brine (15 mL), dried over Na2SO4, filtered, and concentrated. Purification by flash chromatography with 0% to 50% EtOAc/hexanes afforded [3-(methylthio)-5-(trifluoromethyl)phenyl]-methanol. The [3-(methylthio)-5-(trifluoromethyl)phenyl]methanol was contaminated with minor impurities that were removed after the next step. Rf=0.53 (50% EtOAc/hexanes). 1H NMR (CDCl3, 500 MHz) δ 7.63 (s, 1H), 7.40 (s, 1H), 7.35 (s, 1H), 4.71 (s, 2H), 2.51 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737295B2
Source datasetuspto-grants-2010_06
ORD IDord-1da571ec2709469d8671e84f4069c2ac
Source noteuspto-grants-2010_06