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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236100Generated: October 31, 2026

Phenol → HCID 20218023, compound

https://huagongshe.com/reaction/236100

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 hydrochloride salt as in Intermediate 33, m.p. 198°-200° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04642348
Source datasetuspto-grants-1987_02
ORD IDord-130ed77f5ce8490792b92bec26295b8b
Source noteuspto-grants-1987_02