HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413204Generated: October 26, 2026
Furfural → 2-(1-Hydroxy-2-methyl-3-butynyl)-furan
https://huagongshe.com/reaction/2413204
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Furfural | HCID 7362 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Aluminum | HCID 5359268 | — |
| Reactant | 3-Bromo-1-butyne | HCID 10942465 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(1-Hydroxy-2-methyl-3-butynyl)-furan | HCID 13362850 | 58% |
Reaction Steps
Aluminum (5.0 g, 0.18 mole), mercuric chloride (100 mg) and tetrahydrofuran (THF) (70 ml) were added to a reactor, and a solution of 3-bromo-1-butyne (20 g, 0.15 mole) in THF (20 ml) was added dropwise at 40° to 50° C. to prepare a Grignard reagent. Thereafter, to this THF solution of the Grignard reagent was added dropwise a solution of furfural (11.5 g, 0.12 mole) in THF (20 ml) at 20° to 30° C. over about 1 hour, followed by stirring at room temperature for further 2 hours. After completion of the reaction, the reaction solution was poured into an aqueous ammonium chloride solution (about 100 ml) and extracted with ether. The extract was washed with water, dried and concentrated. The residue obtained was distilled under reduced pressure to obtain 10.4 g (yield, 58%) of pure 1-(2-furyl)-2-methyl-3-butyn-1-ol having a boiling point of 75°-85° C./3 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04496586 |
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| Source dataset | uspto-grants-1985_01 |
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| ORD ID | ord-b19be6b3b0944811b2c6cb4c85e6b0c3 |
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| Source note | uspto-grants-1985_01 |
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