HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745245Generated: October 30, 2026
Water → (3-methoxy-4-methylphenyl)methanol
https://huagongshe.com/reaction/745245
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 4-Methyl-m-anisic acid | HCID 81579 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-methoxy-4-methylphenyl)methanol | HCID 11744818 | 83% |
Reaction Steps
Into a solution of 10.0 g of 3-methoxy-4-methylbenzoic acid in 100 ml of dried tetrahydrofuran, while being cooled in ice and stirred under a nitrogen stream, was added dropwise over a period of 15 minutes 80 ml of a 1M solution of borane-tetrahydrofuran complex in tetrahydrofuran. The mixture was then stirred at room temperature for 3 hours. After addition of 10 ml of water, the reaction mixture was stripped of the solvent by distillation. The residue was dissolved in ether, washed with saturated aquecus sodium bicarbonate solution, then with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and stripped of the solvent by distillation to yield 7.6 g of 3-methoxy-4-methylbenzyl alcohol in the form of yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04598077 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-cba8e561ae12412a93e0ec96a972bd30 |
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| Source note | uspto-grants-1986_07 |
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