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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65290Generated: October 29, 2026

Hydrochloric Acid → 4-(3-Cyclopenten-1-ylmethyl)-4'-hydroxy-1,1'-biphenyl

https://huagongshe.com/reaction/65290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant(3-Cyclopenten-1-yl)(4'-methoxy-[1,1'-biphenyl]-4-yl)-methanoneHCID 20234281—
SolventWaterHCID 962—
SolventDiethylene GlycolHCID 8117—
Product4-(3-Cyclopenten-1-ylmethyl)-4'-hydroxy-1,1'-biphenylHCID 20234345—

Reaction Conditions

Temperature200 °C

Reaction Steps

A mixture of (3-cyclopenten-1-yl)(4'-methoxy-[1,1'-biphenyl]-4-yl)-methanone (30 g), hydrazine hydrate (36 ml) and potassium hydroxide (36 g) in 2,2'-oxybisethanol (250 ml) was heated gently, at reflux temperature for 45 min. The low boiling material was distilled off and the mixture was heated under reflux, at 200° C. for 2 h. The cooled reaction mixture was poured into water, acidified with dilute hydrochloric acid and the resulting light brown precipitate was filtered off. This solid was dissolved in methylene dichloride. The solution was washed twice with water and dried (MgSO4), and the solvent was removed. Trituration of the residue with light petroleum gave 4-(3-cyclopenten-1-ylmethyl)-4'-hydroxy-1,1'-biphenyl as a buff solid (25.5 g). A small sample, recrystallised from ether-light petroleum had m.p. 138°-140° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04613619
Source datasetuspto-grants-1986_09
ORD IDord-082980ae059a41dbbd3375aa8ea50ec3
Source noteuspto-grants-1986_09