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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480669Generated: October 31, 2026

Thiourea → HCID 58442454, compound

https://huagongshe.com/reaction/1480669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioureaHCID 2723790—
ReactantHCID 15725271HCID 15725271—
SolventEthanolHCID 702—
ProductHCID 58442454HCID 5844245425.5%

Reaction Steps

A mixture of 2-bromo-1-(2,4,6-triisopropylphenyl)ethanone (13.9 g, 42.7 mmol) and thiourea (3.24 g, 42.6 mmol) in 95% EtOH (60.9 mL) was heated at reflux overnight. The solution was concentrated and added with water (100 mL), saturated aqueous Na2CO3 (10 mL), and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous MgSO4(s), and concentrated under reduced pressure, which was purified by column chromatography on silica gel (33% EtOAc in hexanes as eluant) to give 4-(2,4,6-triisopropylphenyl)thiazol-2-amine (3.28 g) as white solids in 25% yield: 1H NMR (500 MHz, CDCl3) δ 7.03 (s, 2H), 6.22 (s, 1H), 4.75 (bs, 2H), 2.89 (m, 1H), 2.68 (m, 2H), 1.27-1.14 (m, 18H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409902B2
Source datasetuspto-grants-2016_08
ORD IDord-b11d0d2393514834b30ae103b1dbd9ce
Source noteuspto-grants-2016_08