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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1082017Generated: October 29, 2026

Hydrochloric Acid → 4'-(Hydroxymethyl)-[1,1'-Biphenyl]-2-Carboxylic Acid

https://huagongshe.com/reaction/1082017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
Reactant4,4-Dimethyl-2-(4'hydroxymethylbiphenyl-2-yl)oxazolineHCID 11065876—
Product4'-(Hydroxymethyl)-[1,1'-Biphenyl]-2-Carboxylic AcidHCID 1538088081%

Reaction Steps

2.0 g (7.11 mmol) of 4,4-dimethyl-2-(4'-hydroxymethylbiphenyl-2-yl)oxazoline was dissolved in ethanol (30 ml). 2N hydrochloric acid (10 ml) was added thereto, followed by heating under reflux for 3 hours. After the reaction liquid was cooled and concentrated, a saturated aqueous solution of sodium hydrogencarbonate (100 ml) was added thereto, followed by the extraction with chloroform. After the organic phase was washed with water and dried, it was subjected to vacuum concentration. A 20% aqueous solution of sodium hydroxide (20 ml) and ethanol (20 ml) were added to the residue, followed by heating under reflux for 8 hours. After the reaction liquid was cooled to room temperature and adjusted to pH 6 with hydrochloric acid, it was extracted with chloroform. After the organic phase was washed with water and dried, it was subjected to vacuum concentration. The residue was purified by silica gel column chromatography (a chloroform/methanol system) to give 1.31 g of the title compound (yield 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587504
Source datasetuspto-grants-1996_12
ORD IDord-67f3cf6008654bd886a817da4b06039c
Source noteuspto-grants-1996_12