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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840619Generated: November 2, 2026

Phenyl isocyanate → HCID 23448222, compound

https://huagongshe.com/reaction/1840619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl isocyanateHCID 7672—
ReactantHeptaneHCID 8900—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 69689001HCID 69689001—
SolventDichloromethaneHCID 6344—
ProductHCID 23448222HCID 23448222—

Reaction Steps

7.55 mL (103.4 mmol) of thionyl chloride were added dropwise to a suspension of 14.07 g (51.7 mmol) of 4-(3-phenylureido)-3-methoxybenzyl alcohol (prepared as described in Example 1, phenyl isocyanate being employed instead of 2-methylphenyl isocyanate) in 200 mL of dichloromethane. The mixture then was stirred at room temperature for 2 hours, allowed to stand overnight and poured onto 800 mL of heptane. The heptane was decanted off from the separated oil, the residue was suspended several times in heptane and in each case the heptane was decanted off. The residue was dissolved in 100 mL of dichloromethane and added dropwise to 800 mL of diisopropyl ether. The mixture was stirred for 1 hour with ice cooling, and the product was filtered off with suction, washed with diisopropyl ether and dried in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06680333B2
Source datasetuspto-grants-2004_01
ORD IDord-640a1a798f314cf08ee44b2075af35b8
Source noteuspto-grants-2004_01