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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1498903Generated: November 1, 2026

Lawesson's reagent → 4-Chloro-2-methoxythiobenzamide

https://huagongshe.com/reaction/1498903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLawesson's reagentHCID 87949—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 19741766HCID 19741766—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-2-methoxythiobenzamideHCID 63094360129.9%

Reaction Steps

In tetrahydrofuran (100 ml), 4-chloro-2-methoxybenzamide (9.40 g, 50.6 mmol) prepared in the Step 7-1-1 and Lawesson's reagent (10.2 g, 25.3 mmol) were suspended, and the suspension was heated under reflux for 2 hours. After the suspension was allowed to cool, a saturated sodium bicarbonate solution was added to the suspension to stop the reaction. Then the reaction mixture was subjected to extraction with ethyl acetate, and the extract was dried over anhydrous magnesium sulfate and then concentrated. The concentrate was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:1) to give the title compound (6.63 g, 65%) as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09200008B2
Source datasetuspto-grants-2015_12
ORD IDord-f325de120afe492fab11fab3b79ce444
Source noteuspto-grants-2015_12