Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974025Generated: October 30, 2026

4-Hydroxybiphenyl → HCID 15675493, compound

https://huagongshe.com/reaction/974025

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybiphenylHCID 7103—
ReactantSodium HydroxideHCID 14798—
ReactantHeptanenitrile, 7-bromo-HCID 88737—
ReactantHCID 15675492HCID 15675492—
SolventEthylene GlycolHCID 174—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventMethanol--water (1/1)HCID 22242641—
ProductHCID 15675493HCID 1567549397%

Reaction Steps

By the method of Example 34, 7-([1,1'-biphenyl]-4-yloxy)-heptanenitrile was prepared from 7-bromoheptanenitrile and 4-phenylphenol, as shiny flakes from water-methanol, mp 78°-79° C. This material (3.0 g, 10.7 mmol) was heated in ethylene glycol (100 g) containing water (33 ml) and NaOH (10 g). After four hours at reflux, during which the nitrile dissolved and a solid formed, the mixture was cooled, diluted with water (400 ml), and acidified with acetic acid (100 ml). The precipitate was collected by filtration, and dried in vacuo to provide 7-([1,1'-biphenyl]-4-yloxy)heptanoic acid as a white solid (3.1 g 97% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05066658
Source datasetuspto-grants-1991_11
ORD IDord-0039760ae81f407b828110c00bac31a9
Source noteuspto-grants-1991_11