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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840615Generated: November 2, 2026

2-Tolyl isocyanate → 4-(3-(2-Methylphenyl)ureido)-3-methoxybenzyl alcohol

https://huagongshe.com/reaction/1840615

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Tolyl isocyanateHCID 69194—
Reactant3-Methoxy-4-nitrobenzyl alcoholHCID 602961—
CatalystPalladiumHCID 23938—
Solventtert-Butyl methyl etherHCID 15413—
Product4-(3-(2-Methylphenyl)ureido)-3-methoxybenzyl alcoholHCID 11392028—

Reaction Steps

15 g (81.8 mmol) of 3-methoxy-4-nitrobenzyl alcohol were hydrogenated over 1.3 g of palladium/carbon (10% strength; 50% water) in 500 mL of methyl tert-butyl ether with ice cooling. After the absorption of hydrogen was complete, the catalyst was filtered off and 10.14 mL (81.8 mmol) of 2-methylphenyl isocyanate were added to the filtrate with stirring in the course of 30 minutes. The reaction mixture was allowed to stand overnight, and the precipitated solid was filtered off with suction and washed with methyl tert-butyl ether. Yield: 20.5 g (88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06680333B2
Source datasetuspto-grants-2004_01
ORD IDord-45de41897c1540068eafb31c8f8ea975
Source noteuspto-grants-2004_01