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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457569Generated: October 30, 2026

Phenyl isocyanate → [2-(3-Phenylureido)-4-methoxy-6-tert-butylphenoxy]methoxymethane

https://huagongshe.com/reaction/1457569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl isocyanateHCID 7672—
Reactant(2-Amino-4-methoxy-6-tert-butylphenoxy)methoxymethaneHCID 18765846—
SolventTetrahydrofuranHCID 8028—
Product[2-(3-Phenylureido)-4-methoxy-6-tert-butylphenoxy]methoxymethaneHCID 2209942464%

Reaction Steps

A tetrahydrofuran (THF) (20 ml) containing 2.4 g of (2-amino-4-methoxy-6-tert-butylphenoxy)methoxymethane and 1.09 ml of phenyl isocyanate was stirred at room temperature for 3 hours, and then the solvent was removed under reduced pressure. The obtained residue was crystallized from hexane, and recrystallized from an ethyl acetate-hexane mixed solution to give 2.3 g of [2-(3-phenylureido)-4-methoxy-6-tert-butylphenoxy]methoxymethane (yield: 64%, melting point: 121°-123° C., IR: 3300, 1650 cm31 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849732
Source datasetuspto-grants-1998_12
ORD IDord-8fb493ca76e141acaafdcd7cb1679df2
Source noteuspto-grants-1998_12