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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322273Generated: October 26, 2026

1,3-Dichloroacetone → 4-(Chloromethyl)-2-(thiophen-2-yl)-1,3-oxazole

https://huagongshe.com/reaction/322273

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DichloroacetoneHCID 10793—
ReactantPotassium CarbonateHCID 11430—
Reactant2-ThiophenecarboxamideHCID 22063—
SolventWaterHCID 962—
Product4-(Chloromethyl)-2-(thiophen-2-yl)-1,3-oxazoleHCID 252953157%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 2-thiophenecarboxamide (5.09 g) and 1,3-dichloroacetone (457 g) was stirred at 120° C. for 2 hours. The reaction mixture was poured into water, nautralized with potassium carbonate, and then extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried (MgSO4), and concentrated under reduced pressure. The residue was subjected to a silica gel column chromatography. From the fraction eluted with diethyl ether-hexane (1:9, v/v), 4-chloromethyl-2-(2-thienyl)oxazole (4.09 g, 57%) was obtained. Recrystallization from isopropylether gave colorless needles, mp 59-59° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211215B1
Source datasetuspto-grants-2001_04
ORD IDord-c0f2cf7c7df84db1a690d728e4081640
Source noteuspto-grants-2001_04