Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | Heptane | HCID 8900 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 69689001 | HCID 69689001 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23448222 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06680333B2 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-640a1a798f314cf08ee44b2075af35b8 |
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| Source note | uspto-grants-2004_01 |
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