HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579703Generated: November 2, 2026
Methyl Isocyanate → HCID 20136106, compound
https://huagongshe.com/reaction/579703
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | HCID 20136105 | HCID 20136105 | — |
| Catalyst | Diazabicyclo(2.2.2)octane | HCID 136165 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 20136106 | HCID 20136106 | 93.5% |
Reaction Steps
27.5 g (0.10 mol) of 3-(4-chloro-2-fluoro-5-methoxyphenyl)-4-hydroxy-1-methylimidazolidin-2-one (Example 1) are dissolved in 200 ml of acetonitrile, 50 mg of diazabicyclo[2.2.2]octane are added, and 6.84 g (0.12 mol) of methyl isocyanate are added dropwise at 20° C. The mixture is stirred for 5 hours at 50° C. and the solvent is removed by distillation. The solid residue which remains is boiled up in 200 ml of ether and cooled in an ice-bath. The precipitate is filtered off under suction and dried. 31.0 g (93% of theory) of 3-(4-chloro-2-fluoro-5-methoxyphenyl)-1-methyl-4-(N-methylcarbamoyloxy)imidazolidin2-one are obtained in the form of colorless crystals having the melting point 128°-131° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04749403 |
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| Source dataset | uspto-grants-1988_06 |
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| ORD ID | ord-0eb699db8def4736890ea8ee6bfdbdc8 |
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| Source note | uspto-grants-1988_06 |
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