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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613238Generated: November 2, 2026

Water → HCID 19775579, compound

https://huagongshe.com/reaction/1613238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 19775538HCID 19775538—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
ProductHCID 19775579HCID 1977557921.6%

Reaction Steps

3 g of ethyl 4-[[4-propyl-5-(4-nitrobenzyl)thiazol-2-yl]mercapto]butyrate in 50 ml of ethanol are hydrogenated at normal pressure and room temperature in the presence of Raney nickel. After filtration of the catalyst and concentration of the filtrate, the brown oil obtained is taken up with acidified water. The aqueous phase is extracted with chloroform, rendered basic with dilute sodium hydroxide and extracted with ether. The ether solution is dried and concentrated to give a yellow oil, which is purified on a silica column (eluent: 7/3 cyclohexane/ethyl acetate) to give 0.6 g of ethyl 4-[[4-propyl-5-(4-aminobenzyl)thiazol-2-yl]mercapto]butyrate in the form of a pink oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05192781
Source datasetuspto-grants-1993_03
ORD IDord-45907f4e55564882a1e535bd9ca27cdb
Source noteuspto-grants-1993_03