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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2,4-Dimethyl-3-hydroxymethyl-5-iodothiophene | HCID 12875267 | — |
| Product | 2,4-Dimethyl-3-hydroxymethyl-5-methoxythiophene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04061656 |
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| Source dataset | uspto-grants-1977_12 |
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| ORD ID | ord-52a4777bfd7e4e0787e492845b5411d6 |
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| Source note | uspto-grants-1977_12 |
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