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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256157Generated: October 30, 2026

Sodium Thiosulfate → HCID 86655224, compound

https://huagongshe.com/reaction/1256157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 86655225HCID 86655225—
SolventDichloromethaneHCID 6344—
ProductHCID 86655224HCID 8665522489%

Reaction Steps

A solution of 2,2,2-trifluoro-N-(3-(2-(methylthio)ethyl)phenyl)acetamide (4 g, 15 mmol) and m-CPBA (7.9 g, 45 mmol) in DCM (30 mL) was heated to reflux overnight. Aqueous solution of sodium thiosulfate (10 mL) was added. The solid was filtered from the mixture solution. The aqueous layer was extracted by ethyl acetate 3 times. The combined organic phase was washed with brine, dried over sodium sulfate and concentrated to give 2,2,2-trifluoro-N-(3-(2-(methylsulfonyl)ethyl)phenyl)acetamide (4 g, yield 89%). 1H NMR: 400 MHz CDCl3 δ 7.85 (s, 1H), 7.50-7.49 (m, 1H), 7.36-7.28 (m, 2H), 7.07-7.05 (m, 1H), 3.26-3.22 (m, 2H), 3.14-3.10 (m, 2H), 2.79 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461134B2
Source datasetuspto-grants-2013_06
ORD IDord-0781e7cbc57042d48b233e8381c0f2e7
Source noteuspto-grants-2013_06