Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995118Generated: October 30, 2026

Hydrochloric Acid → [1,1'-Biphenyl]-3-methanol, 2-methyl-

https://huagongshe.com/reaction/1995118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Methyl-3-nitrobenzyl alcoholHCID 90289—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
Product[1,1'-Biphenyl]-3-methanol, 2-methyl-HCID 596875—
Product(3-Amino-2-methylphenyl)methanol hydrochlorideHCID 20270659—

Reaction Steps

2-Methyl[1,1'-biphenyl]-3-methanol was prepared as follows: To 100 ml of stirred 50% aqueous ethanol was added 2-methyl-3-nitrobenzyl alcohol (41.8 g, 0.25 mole) and 85.0 grams of iron powder. The mixture was brought to reflux, and 5.2 ml of concentrated hydrochloric acid was slowly added. Upon complete addition, the reaction mixture was stirred under reflux for 2 hours. The reaction mixture was then made just basic with ethanolic 15% potassium hydroxide. The hot mixture was filtered through diatomaceous earth to remove the iron. The filter cake was washed with ethanol. The filtrate was acidified with hydrogen chloride, then allowed to stand at room temperature for 16 hours. The ethanol was removed by evaporation under reduced pressure. Hexane was added to the residue, and the water-hexane azeotrope was removed by distillation. The addition of hexane and the subsequent removal of the water-hexane azeotrope by distillation was repeated three times. The 3-hydroxymethyl-2-methylaniline hydrochloride residue thus obtained was used as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04402973
Source datasetuspto-grants-1983_09
ORD IDord-6f6a66ef10ad4cc0bfad7ac68c0e6712
Source noteuspto-grants-1983_09