HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541166Generated: October 26, 2026
Water → 3-(Benzyloxy)-4-methoxybenzyl alcohol
https://huagongshe.com/reaction/541166
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 3-Benzyloxy-4-methoxybenzaldehyde | HCID 80671 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-(Benzyloxy)-4-methoxybenzyl alcohol | HCID 74622 | — |
| Product | 3-Hydroxy-4-methoxybenzyl alcohol | HCID 78089 | — |
Reaction Steps
121.1 mg (0.50 mmol) of 3-benzyloxy-4-methoxybenzaldehyde (7), 270 μL (15 mmol) of distilled water and stainless steel balls (50 pieces) were placed in the vessel of the planetary ball mill, which was then closed, and agitated by operating the planetary ball mill for 12 hours at 800 rpm (reversed every 30 minutes). After the lapse of 12 hours, 10 mL of ethyl acetate was added to the vessel of the ball mill to provide a solution containing the reaction mixture, which was then filtered with celite. The operation was repeated 5 times to provide a filtrate, which was then concentrated, thereby providing 74.0 mg (0.31 mmol) of 3-benzyloxy-4-methoxybenzyl alcohol (8) and 6.9 mg (0.05 mmol) of 3-hydroxy-4-methoxybenzyl alcohol (9). The yields were 61% and 9%, respectively. The reaction is expressed by the following scheme. 23.7 mg (0.10 mmol) of unreacted 3-benzyloxy-4-methoxybenzaldehyde (7) was recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871980B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-2e7f6a84271b4e71b532d9f211b0340c |
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| Source note | uspto-grants-2014_10 |
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