HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482828Generated: October 30, 2026
Benzyl Alcohol → 3-(Benzyloxy)propanoic acid
https://huagongshe.com/reaction/482828
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Methyl Acrylate | HCID 7294 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 3-(Benzyloxy)propanoic acid | HCID 15608813 | — |
Reaction Steps
A mixture of benzyl alcohol (84 ml) and methyl acrylate (80.6 ml) is then added drop by drop to the stirred solution over a period of 20-30 minutes, and stirring is continued for additional 20 minutes. Once the reaction, which is monitored by gas chromatography, is completed, 4N KOH (500 ml) is added and the mixture is stirred at room temperature for 2 hours. Then, 8% HCl (420 ml) is added keeping the temperature at about 20°-25° C. and the mixture is extracted with methylene chloride (200 ml plus four 50-ml portions). The mother liquors are acidified with 37% HCl (102 ml) to reach a pH of about 2.5 and extracted again with toluene (200 ml plus three 100 ml portions) The toluene extracts are combined, dried over Na2SO4, and concentrated to dryness yielding an oily residue of 3-benzyloxypropionic acid (100 g) which is employed as such in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04576746 |
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| Source dataset | uspto-grants-1986_03 |
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| ORD ID | ord-ea4b765aaa834a11bb404f89fa3955a1 |
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| Source note | uspto-grants-1986_03 |
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