HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086323Generated: November 1, 2026
Ethyl vinyl ether → 4-[2-(Ethenyloxy)ethyl]phenol
https://huagongshe.com/reaction/2086323
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl vinyl ether | HCID 8023 | — |
| Reactant | Tyrosol | HCID 10393 | — |
| Catalyst | Mercurous acetate | HCID 61181 | — |
| Product | 4-[2-(Ethenyloxy)ethyl]phenol | HCID 15496510 | 60% |
Reaction Steps
4-Hydroxyphenethyl alcohol of formula 3a (15.0 g, 108.0 mmol) was added to ethylvinyl ether of formula 4(200 ml) and stirred for 20 minutes. After cooling to 0° C., mercury acetate (3.4 g, 10.8 mmol) was added and the reaction mixture was stirred for 24 hrs at room temperature. After evaporating solvent, the residue was purified by fresh column chromatography on silica gel (hexane/ethylacetate=5/1, v/v) to obtain pale yellow liquid of the desired product, 4-(2-vinyloxyethyl)phenol of formula 5a (11.0 g, 65 mmol, yield 60%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06723798B1 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-9221772d99e7422d96a670f9e7ad2c2e |
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| Source note | uspto-grants-2004_04 |
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