HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441415Generated: October 30, 2026
4-Hydroxybenzyl Alcohol → 2-(4-Phenoxymethylphenoxy)-propionic acid
https://huagongshe.com/reaction/441415
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzyl Alcohol | HCID 125 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | Ethyl 2-bromopropionate | HCID 79040 | — |
| Reactant | 2-[4-(Hydroxymethyl)phenoxy]propanoic acid | HCID 351924 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2-(p-Bromoethylphenoxy)-propionic acid | HCID 57189959 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-Phenoxymethylphenoxy)-propionic acid | HCID 21421173 | — |
Reaction Steps
2.3 g. of sodium is dissolved in 250 ml. of absolute ethanol; 9.4 g. of phenol and 28.6 g. of the ethyl ester of 2-(p-bromoethylphenoxy)-propionic acid [obtainable by reacting p-hydroxybenzyl alcohol with ethyl 2-bromopropionate to the ethyl ester of 2-(p-hydroxymethylphenoxy)-propionic acid and subsequent reaction with SOBr2 ] are added thereto, and the mixture is refluxed for 3 hours and evaporated. The usual working-up procedure yields the ethyl ester of 2-(4-phenoxymethylphenoxy)-propionic acid. Analogously, the ethyl ester of 2-(4-phenoxymethylphenoxy)-2-methylpropionic acid is obtained from the ethyl ester of 2-p-bromomethylphenoxyisobutyric acid (obtainable by bromination of the ethyl ester of 2-p-methylphenoxyisobutyric acid with N-bromosuccinimide);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04039683 |
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| Source dataset | uspto-grants-1977_08 |
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| ORD ID | ord-61e8a8cd51c44809b1f1726acb960e76 |
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| Source note | uspto-grants-1977_08 |
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