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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613252Generated: November 1, 2026

(Methylthio)thioacetamide → 2-Methylthiomethyl-5-(4-nitrobenzyl)-4-propylthiazole

https://huagongshe.com/reaction/1613252

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Methylthio)thioacetamideHCID 19014065—
ReactantHCID 19775543HCID 19775543—
SolventCyclohexane ethylacetateHCID 21867204—
Product2-Methylthiomethyl-5-(4-nitrobenzyl)-4-propylthiazoleHCID 1977557586.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 5 g of 2-chloro-1-(4-nitrophenyl)-hexan-3-one (0.02 mol) and 2.6 g of (methylthio)thioacetamide (0.022 mol) is heated at 60° C. for 24 h. The reaction is followed by TLC (7/3 cyclohexane/ethyl acetate). The reaction medium is then treated according to the process of Example 45 to give 5.6 g of 2-methylthiomethyl-5-(4-nitrobenzyl)-4-propylthiazole in the form of an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05192781
Source datasetuspto-grants-1993_03
ORD IDord-70bb8c6cf0e14e1b83537ca32639d6a9
Source noteuspto-grants-1993_03