Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591536Generated: November 1, 2026

Sulfuric Acid → 4-(Chloromethyl)-2-methyl-1,3-thiazole

https://huagongshe.com/reaction/1591536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant1,3-DichloroacetoneHCID 10793—
Reactant4-(Chloromethyl)-2-methyl-1,3-thiazoleHCID 736341—
ReactantThioacetamideHCID 2723949—
CatalystHCID 178418406HCID 178418406—
Product4-(Chloromethyl)-2-methyl-1,3-thiazoleHCID 736341—
ProductHCID 68446013HCID 68446013—

Reaction Steps

According to the description in J. Heterocyclic Chem., 1979, 16, 1563, 4-chloromethyl-2-methylthiazole was synthesized with 1,3-dichloroacetone and thioacetamide as starting materials. The above-obtained 4-chloromethyl-2-methylthiazole was converted to a 4-hydroxymethyl body by dilute sulfuric acid, and then introduced into a 4-formyl body by oxidation of manganese dioxide (yield to this point: 62%). 5-Ethoxycarbonyl-2-methylpyrrolo[3,2-d]thiazole was obtained by making ethyl azidoacetate act on the above product in the presence of sodium ethoxide and further heating in xylene (yield: 31%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291449B2
Source datasetuspto-grants-2007_11
ORD IDord-a23de3ee6d5646ebb9448c6e78184d51
Source noteuspto-grants-2007_11