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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211112Generated: October 31, 2026

Methanol → HCID 19375608, compound

https://huagongshe.com/reaction/2211112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2-Thiophenecarbonyl chlorideHCID 78928—
ReactantHCID 12694430HCID 12694430—
ReactantCID 53628100HCID 178418400—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19375608HCID 1937560887.1%

Reaction Steps

2.0 g of 2-(3-thienyl)-4,4-dimethyloxazoline was dissolved in 50 ml of ether, and 10 ml of s-butyllithium (1.3M, cyclohexane solution) was added dropwise thereto at -70° C. The solution was stirred for 1 hour. The reaction solution was added dropwise to a solution of 2.4 g of 2-thenoyl chloride in 50 ml of tetrahydrofuran at -78° C., and the solution was stirred for 30 minutes. Thereafter, 1 ml of methanol was added to the solution, and the reaction solution was concentrated. After adding water thereto, the solution was extracted with chloroform. The chloroform layer was dried and concentrated, and the residue was purified by silica gel chromatography to obtain 2.8 g of 2-(2-thenoyl)-3-(4,4-dimethyl-2-oxazoline-2-yl)thiophene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05462941
Source datasetuspto-grants-1995_10
ORD IDord-60e3e00f38ba4cd7b7559c8be7bda3ac
Source noteuspto-grants-1995_10