HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764125Generated: October 26, 2026
Anisole, p-1-cyclohexen-1-yl- → Phenol, p-(1-cyclohexen-1-yl)-
https://huagongshe.com/reaction/1764125
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Anisole, p-1-cyclohexen-1-yl- | HCID 253825 | — |
| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Solvent | Water | HCID 962 | — |
| Product | Phenol, p-(1-cyclohexen-1-yl)- | HCID 69727 | — |
Reaction Steps
56.5 Grams of p-(1-cyclohexenyl)-anisol and 125 g of pyridine-hydrochloride are thoroughly mixed and heated for 3 hours in an atmosphere of nitrogen to 180° C. The reaction mixture is cooled to room temperature, treated with water and extracted with 3 × 400 ml of benzene. The benzene extracts are washes with 3 × 300 ml of water, dried over sodium sulphate and evaporated in vacuo. The solid residue yields the crude p-(1-cyclohexenyl)-phenol (m.p. 115-119° C), which can be purified by recrystallisation from benzene and then melts at 120°-122° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04115416 |
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| Source dataset | uspto-grants-1978_09 |
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| ORD ID | ord-7a63c0b80e93477dbaade6ac592abf63 |
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| Source note | uspto-grants-1978_09 |
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