HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883618Generated: November 2, 2026
Acetic Acid → (4-Methylbiphenyl-3-yl)methanol
https://huagongshe.com/reaction/1883618
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2-Methyl-5-phenylbenzaldehyde | HCID 12056529 | — |
| Reactant | HCID 178418435 | HCID 178418435 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | (4-Methylbiphenyl-3-yl)methanol | HCID 12056528 | — |
Reaction Steps
123 g (625 mmol) of 2-methyl-5-phenylbenzaldehyde was dissolved in a mixture of 1.1 L of tetrahydrofuran and 110 ml of water, and to the resulted solution was dropped, at 15 to 20° C., a solution prepared by dissolving 7.7 g (203 mmol) of sodium boron hydride in 70 ml of a 0.1 wt % sodium hydroxide aqueous solution. After completion of dropping, the mixture was stirred for 4 hours at 15 to 20° C. To this reaction solution was dropped 10 g of glacial acetic acid at 20° C. or lower, and this was poured into ice water. The reaction solution was extracted with t-butyl methyl ether, the organic layer was washed with water, saturated sodium bicarbonate solution, then, saturated saline, dried over anhydrous magnesium sulfate, then, concentrated to obtain 121 of 2-methyl-5-phenylbenzyl alcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06762197B2 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-4bcacee149ec4da088bc4aad7a767d4a |
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| Source note | uspto-grants-2004_07 |
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