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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373848Generated: November 1, 2026

Ammonia → Methyl 4-(thioureidomethyl)benzoate

https://huagongshe.com/reaction/1373848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantTriethylamineHCID 8471—
Reactant1,1'-ThiocarbonyldiimidazoleHCID 80264—
ReactantMethyl 4-(aminomethyl)benzoate hydrochlorideHCID 2729253—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventHexaneHCID 8058—
ProductMethyl 4-(thioureidomethyl)benzoateHCID 2302399491.3%

Reaction Steps

Under an argon atmosphere, to a suspension of methyl 4-aminomethylbenzoate hydrochloride (170.0 g, 0.843 mol) in chloroform (850 ml, 5.0 v/w) were successively added 1,1′-thiocarbonyldiimidazole (purity 90%, 166.0 g, 0.843 mol) and triethylamine (123 ml, 0.885 mol). After stirring at room temperature for 3 hr, 28% aqueous ammonia (570 ml, 8.43 mol) and methanol (170 ml, 1.0 v/w) were added and the mixture was stirred overnight. n-Hexane (1700 ml, 10.0 v/w) and water (850 ml, 5.0 v/w) were successively added to the reaction mixture and the mixture was stirred at room temperature for 3 hrs. The precipitated crystals were collected by filtration, washed successively with n-hexane (500 ml) and water (500 ml) and dried in vacuo to give the title compound (172.5 g, yield 91.3%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163952B2
Source datasetuspto-grants-2007_01
ORD IDord-133213ae01a14a64b0ae04128d89c078
Source noteuspto-grants-2007_01