HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 617663Generated: October 25, 2026
Hydrochloric Acid → Allyl 4-hydroxymethylbenzoate
https://huagongshe.com/reaction/617663
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 4-(hydroxymethyl)benzoate | HCID 81325 | — |
| Product | Allyl 4-hydroxymethylbenzoate | HCID 22392687 | 93% |
Reaction Steps
To an alkoxide solution prepared from sodium hydride (60% in oil, 1.60 g, 40.0 mmol) and allyl alcohol (100 mL) was added methyl 4-hydroxymethylbenzoate (3.32 g, 20.0 mmol) under ice-cooling. The resulting mixture was stirred at room temperature for 6 h, adjusted with 1N hydrochloric acid to pH 3, and then concentrated under reduced pressure. To the residue was added ethyl acetate (150 mL), and the mixture was washed successively with 1N hydrochloric acid, saturated aqueous sodium hydrogencarbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was separated and purified by silica gel column chromatography (hexane-ethyl acetate, 5:2) to give 3.59 g (93%) of allyl 4-hydroxymethylbenzoate as a pale-yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05948785 |
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| Source dataset | uspto-grants-1999_09 |
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| ORD ID | ord-db83d4d35d4149a88a32754fd30c5845 |
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| Source note | uspto-grants-1999_09 |
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