HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589988Generated: November 1, 2026
Hydrochloric Acid → Ethyl 2-hydroxy-6-vinylbenzoate
https://huagongshe.com/reaction/1589988
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (3-Acetyloxy-2-ethoxycarbonylbenzyl)-triphenylphosphonium bromide | HCID 10929793 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 2-hydroxy-6-vinylbenzoate | HCID 15008897 | — |
Reaction Steps
A solution of 12.7 g of sodium carbonate in 115 ml of water was added dropwise, while stirring vigorously at room temperature, to 33.8 g of (3-acetoxy-2-ethoxycarbonylbenzyl) triphenylphosphonium bromide (e.g. Eicher et al. Synthesis (1988) 525) in 264 ml of 36.5% by weight aqueous formaldehyde solution. The reaction mixture was stirred at 55° C. for 6 h and then poured into ice-water at pH 1 (hydrochloric acid) and extracted with ethyl acetate, after which the combined organic phases were dried over sodium sulfate and concentrated under reduced pressure. Further purification was carried out by chromatography on silica gel with toluene/ethyl acetate (20:1) as eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05201937 |
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| Source dataset | uspto-grants-1993_04 |
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| ORD ID | ord-54034659aed0475bbcda7b9622bb1bd1 |
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| Source note | uspto-grants-1993_04 |
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