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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417295Generated: November 3, 2026

Thiourea → 3-(2-Amino-thiazol-4-yl)-benzonitrile

https://huagongshe.com/reaction/1417295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioureaHCID 2723790—
Reactant3-(2-Bromoacetyl)benzonitrileHCID 2735867—
SolventMethanolHCID 887—
Product3-(2-Amino-thiazol-4-yl)-benzonitrileHCID 2756558—

Reaction Conditions

Temperature0 °C

Reaction Steps

16.9 g of 3-bromoacetyl-benzonitrile were placed in 50 ml of methanol and treated at room temperature with 8 g of thiourea. The mixture was boiled for 2 1/2 hours and then cooled to 0° C. while stirring slowly. The product separated as the salt, was filtered off and converted into the base by the addition of 100 ml of 2N sodium hydroxide solution. The aqueous suspension was extracted with a total of 700 ml of methylene chloride and the organic phase was dried with magnesium sulphate. 9.6 g of 3-(2-amino-thiazol-4-yl)-benzonitrile separated upon concentration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877193
Source datasetuspto-grants-1999_03
ORD IDord-863718259a9f424993102bc40ff1af25
Source noteuspto-grants-1999_03