HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859941Generated: October 31, 2026
Benzyl Bromide → 3-(4-Benzyloxyphenyl)-2-hydroxypropionic acid ethyl ester
https://huagongshe.com/reaction/1859941
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl p-hydroxyphenyllactate | HCID 21930973 | — |
| Product | 3-(4-Benzyloxyphenyl)-2-hydroxypropionic acid ethyl ester | HCID 15186153 | 96.9% |
Reaction Steps
Benzyl bromide (21.9 g) and potassium carbonate (35.3 g) were added to a solution of ethyl 3-(4-hydroxyphenyl)lactate (22.4 g) in dimethylformnamide (220 ml). The mixture was stirred at 50° C. for 2 hours. The reaction mixture was partitioned between ethyl acetate and water. The ethyl acetate layer was separated and dried over magnesium sulfate and then concentrated under reduced pressure. The residue was purified via chromatography silica gel column using hexane/ethyl acetate=7/3 as the eluant to give the desired compound (31.0 g) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06528525B1 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-be8c11a1835a486585b5db781b7789e0 |
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| Source note | uspto-grants-2003_03 |
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