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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285278Generated: November 2, 2026

3-(4-aminophenyl)-1-(4-methylphenyl)propan-1-one → 3-(4-aminophenyl)-1-(4-methylphenyl)propan-1-ol

https://huagongshe.com/reaction/1285278

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-aminophenyl)-1-(4-methylphenyl)propan-1-oneHCID 2768267—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
Product3-(4-aminophenyl)-1-(4-methylphenyl)propan-1-olHCID 4313746—

Reaction Steps

60 g of the 1-(4-methylphenyl)-3-(4-aminophenyl)-n-propan-1-one prepared as described in Example A were hydrogenated, in 1 liter of tetrahydrofuran, in the presence of 5 g of 10% strength Pd on charcoal, under 1.1 bar, until 5.5 liters of hydrogen had been absorbed. The catalyst was separated off and the reaction solution was evaporated down, and the oil obtained crystallized on trituration with diisopropyl ether. After the white crystals had been dried, 53 g (88% of theory) of the carbinol of melting point 63°-65° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04566900
Source datasetuspto-grants-1986_01
ORD IDord-16f89062146b4684aa3f9195002e85bc
Source noteuspto-grants-1986_01