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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnisole, p-1-cyclohexen-1-yl-HCID 253825—
ReactantPyridinium chlorideHCID 10176127—
SolventWaterHCID 962—
ProductPhenol, p-(1-cyclohexen-1-yl)-HCID 69727—

Reaction Conditions

Temperature180 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04115416
Source datasetuspto-grants-1978_09
ORD IDord-7a63c0b80e93477dbaade6ac592abf63
Source noteuspto-grants-1978_09