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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764579Generated: October 31, 2026

Diethyl Ether → 2,4-Dimethylthiophene-3-carbaldehyde

https://huagongshe.com/reaction/1764579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantDimethylformamideHCID 6228—
Reactant3-Bromo-2,4-dimethylthiopheneHCID 10631774—
ReactantButyllithiumHCID 178418339—
SolventHexaneHCID 8058—
Product2,4-Dimethylthiophene-3-carbaldehydeHCID 11147770—

Reaction Conditions

Temperature-20 °C

Reaction Steps

A solution of 15 g. (79.0 mmol) of 2,4-dimethyl-3-bromothiophene in 120 ml. of dry ether was cooled to -70° C. and 36 ml. of a hexane solution of n-butyl lithium (2.4 molar, 86.4 mmol) were added dropwise. The reaction mixture was allowed to warm up to -20° C. for 10 min., cooled again to -70° C. and then quenched by adding dropwise 15 g. (0.205 mol) of dimethylformamide. The mixture was stirred at room temperature overnight, poured into ice water, stirred for 15 min. and extracted four times with ether. The ether phase was washed with saturated sodium chloride solution, dried and evaporated. The resulting oily residue was distilled to yield 2,4-dimethylthiophene-3-carboxaldehyde, b.p. 50°-55° C./0.1 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04116975
Source datasetuspto-grants-1978_09
ORD IDord-52a7df71499f46b4831950f14549fca8
Source noteuspto-grants-1978_09