HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877029Generated: November 2, 2026
Hydrochloric Acid → (2-methyl-5-phenylfuran-3-yl)methanol
https://huagongshe.com/reaction/1877029
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | ethyl 2-methyl-5-phenyl-3-furoate | HCID 10331426 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-methyl-5-phenylfuran-3-yl)methanol | HCID 2776433 | 100.9% |
Reaction Steps
A solution of ethyl 2-methyl-5-phenyl-3-furancarboxylate (5.7 g) in tetrahydrofuran (30 mL) was added dropwise to a suspension of lithium aluminum hydride (1.0 g) in tetrahydrofuran (30 mL) at 0° C. and, after the completion of the dropwise addition, the mixture was stirred at 0° C. for 30 min. The reaction mixture was treated with 1N hydrochloric acid, poured into water, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure to give the title compound (4.7 g, 100%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08309580B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-523c8da57d794baca9819a91d1cf22ce |
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| Source note | uspto-grants-2012_11 |
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