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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460980Generated: October 26, 2026

Methanol → 2,4-Dimethyl-3-hydroxymethyl-5-methoxythiophene

https://huagongshe.com/reaction/460980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodiumHCID 5360545—
Reactant2,4-Dimethyl-3-hydroxymethyl-5-iodothiopheneHCID 12875267—
Product2,4-Dimethyl-3-hydroxymethyl-5-methoxythiopheneHCID 12875268—

Reaction Steps

12.0 G. (0.151 mol) of cupric oxide and 12.5 g. (0.0466 mol) of 2,4-dimethyl-3-hydroxymethyl-5-iodothiophene were added to a solution of 12.5 g. (0.543 mol) of sodium in 100 ml. of dry methanol. The reaction mixture was heated to 80°-82° C. (internal temperature) for 20 hrs. with vigorous stirring, then cooled. The cold solution was diluted with 150 ml. of methanol, filtered, poured into ice water and extracted with ether/hexane (ratio 4:1). The organic layers were washed with 5% sodium carbonate solution, dried and evaporated. The residue which resulted was recrystallized from hexane to yield 2,4-dimethyl-3-hydroxymethyl-5-methoxythiophene, m.p. 55°-60° C. This product contained about 10% of 2,4-dimethyl-3-hydroxymethylthiophene which is formed in this reaction by reduction of the iodide. Fraction recrystallization of a sample from hexane yielded pure 2,4-dimethyl-3-hydroxymethyl-5-methylthiophene, m.p. 64°-65° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04061656
Source datasetuspto-grants-1977_12
ORD IDord-52a4777bfd7e4e0787e492845b5411d6
Source noteuspto-grants-1977_12