HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781167Generated: October 30, 2026
4-Phenoxybenzaldehyde → (4-Phenoxyphenyl)methanol
https://huagongshe.com/reaction/1781167
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Phenoxybenzaldehyde | HCID 66139 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-Phenoxyphenyl)methanol | HCID 826195 | 98.9% |
Reaction Steps
A solution of 4-phenoxybenzaldehyde (10.0 g, 50 mmol) and 10 mL dry THF was added dropwise to a 0° C. suspension of lithium aluminum hydride (2.1 g, 55.3 mmol) and 100 mL dry THF. The reaction mixture was stirred for 1 hour at 0° C., then was quenched successively with 2.1 mL H20, 2.1 mL 10% NaOH, and 6.3 mL H2O. The resultant slurry was stirred for 1.5 hours at room temperature, then was filtered through Celite® and the filtrate was evaporated under reduced pressure to afford the title compound (9.9 g) as a white solid. 1HNMR (300 MHz, CDCl3) δ 1.68 (t, 1H), 4.68 (d, 2H), 7.00 (m, 4H), 7.10 (t, 1H), 7.35 (m, 4H). MS (DCl/NH3) m/e 183 (M+1, -H2O)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05631401 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-738e7cb49cf74664a77d5d70d96138ca |
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| Source note | uspto-grants-1997_05 |
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