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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981798Generated: November 2, 2026

Phenol → HCID 20218023, compound

https://huagongshe.com/reaction/1981798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 13607960HCID 13607960—
SolventHydrogen BromideHCID 260—
ProductHCID 20218023HCID 20218023—

Reaction Steps

A mixture of 200 g (2.13 mole) of phenol, 200 ml of 48% hydrobromic acid and 21.86 g (0.053 mole) of 4-[(2,5-dichlorophenyl)thio]-1-[(4-methylphenyl)sulfonyl]piperidine were heated at reflux for 1.5 hr. The reaction mixture was diluted to 2 liters volume with ice water and made alkaline with 50% sodium hydroxide. The aqueous layer was extracted with diethyl ether. The ether phase was extracted with 1N sulfuric acid. The resulting aqueous acidic phase was extracted with methylene chloride. The methylene chloride phase was dried, filtered and evaporated to remove solvent to give a brown oil, the free base of the title compound. The free base was converted to 9.36 g (59.1%) of a white crystalline hydrochlorid esalt as in Intermediate 33, m.p. 198°-200° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04593102
Source datasetuspto-grants-1986_06
ORD IDord-e303aace9dad49c39d1c5cd11bf1f5fc
Source noteuspto-grants-1986_06