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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401783Generated: October 31, 2026

Thiourea → 4-(4-Chlorobenzyl)thiazol-2-amine

https://huagongshe.com/reaction/2401783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioureaHCID 2723790—
Reactant1-Bromo-3-(4-chlorophenyl)propan-2-oneHCID 14748855—
SolventEthanolHCID 702—
Product4-(4-Chlorobenzyl)thiazol-2-amineHCID 1165150186%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 1-bromo-3-(4-chlorophenyl)propan-2-one (25.4 grams, 103 mmol) and thiourea (8.59 g, 113 mmol) in ethanol (1.51 L) was heated at 85° C. for 2 hours. The reaction was cooled and concentrated in vacuo and the residue was taken up in ethyl acetate (300 mL) and saturated sodium bicarbonate (100 mL). The layers were separated and the aqueous layer was extracted with ethyl acetate (100 mL). The combined organic layers were washed with brine (50 mL), dried over MgSO4, filtered, and concentrated in vacuo. The residue was recrystallized from ethyl acetate/hexanes to give 19.9 grams of the title compound as a tan powder (86% yield). LC/MS (FA) ES+ 225. 1H NMR (300 MHz, CDCl3) δ: 7.29-7.24 (m, 2H), 7.20-7.15 (m, 2H), 6.04 (m, 1H), 5.00 (bs, m, 2H), 3.83 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796268B2
Source datasetuspto-grants-2014_08
ORD IDord-d5f3151751634c669bf29236dbccfee8
Source noteuspto-grants-2014_08