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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066232Generated: October 26, 2026

2-Chloro-1,3-oxazole → 4,5-Dihydro-8-methylthio-2-phenylbenzo[2,1-c:3,4-b']dithiophene-6-carboxamide

https://huagongshe.com/reaction/1066232

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1,3-oxazoleHCID 13371074—
Reactant4,5-Dihydro-8-methylthio-2-phenylbenzo[2,1-c:3,4-b']dithiophene-6-carboxylic acidHCID 18388311—
CatalystDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product4,5-Dihydro-8-methylthio-2-phenylbenzo[2,1-c:3,4-b']dithiophene-6-carboxamideHCID 1838831956%

Reaction Steps

4,5-Dihydro-8-methylthio-2-phenylbenzo[2,1-c:3,4-b′]dithiophene-6-carboxylic acid (0.50 g) was dissolved in tetrahydrofuran (10 ml); oxazolyl chloride (0.15 ml) and then N,N-dimethylformamide (one drop) were added. After the mixture was stirred at room temperature for 2 hours, it was concentrated under reduced pressure. The residue was dissolved in tetrahydrofuran (30 ml); concentrated aqueous ammonia (5 ml) was added. After the reaction mixture was stirred at room temperature for one hour, it was poured over water and extracted with chloroform-methanol the organic layer was washed with water and dried (MgSO4), after which the solvent was distilled off to yield 4,5-dihydro-8-methylthio-2-phenylbenzo[2,1-c:3,4-b′]dithiophene-6-carboxamide (0.28 g, 56%), which was recrystallized from ethanol. Melting point 192-193° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06242471B1
Source datasetuspto-grants-2001_06
ORD IDord-34cc80b2f474430494de1c2d3277ec24
Source noteuspto-grants-2001_06