HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389321Generated: October 29, 2026
Water → Ethyl [3-(3-hydroxypropyl)phenoxy]acetate
https://huagongshe.com/reaction/2389321
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Hydroxybenzenepropanol | HCID 10351871 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl [3-(3-hydroxypropyl)phenoxy]acetate | HCID 86637895 | — |
Reaction Steps
To a solution of 3-(3-hydroxypropyl)phenol (100 g) in MeCN (750 mL) was added K2CO3 (109 g) at ambient temperature. Ethyl bromoacetate (87.4 mL) was added dropwise to the mixture at 0° C. over 30 minutes, and then the mixture was stirred at ambient temperature for 20 hours and at 60° C. for 7 hours. Water (800 mL) was added to the mixture at ambient temperature and the resulting mixture was extracted with EtOAc(1 L) two times. The organic layer was washed with brine, dried over anhydrous MgSO4, filtered and evaporated in vacuo. The residue was purified by silica gel column chromatography (n-hexane:EtOAc=1:1) to afford ethyl [3-(3-hydroxypropyl)phenoxy]acetate (121 g) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08273745B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-d40d2f86f2da46a5af754d1487b39401 |
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| Source note | uspto-grants-2012_09 |
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