Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Carbaryl | HCID 6129 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | 1-Naphthol | HCID 7005 | — |
| Reactant | 2-Naphthol | HCID 8663 | — |
| Reactant | Methylcarbamoyl chloride | HCID 80931 | — |
| Solvent | Cumene | HCID 7406 | — |
| Product | beta-Carbaryl | HCID 77710 | — |
Reaction Steps
A process for the manufacture of α-naphthyl-N-methylcarbamate by the reaction of methylcarbamyl chloride and α-naphthol containing β-naphthol as an impurity, which comprises reacting methylcarbamyl chloride, which is essentially free from phosgene and hydrogen chloride, in the absence of an acid-binding agent, with α-naphthol containing β-naphthol as an impurity at a temperature in the range of 60° to 130° C in, as solvent, cumene, the starting concentration of said naphthol in the cumene being in the range of 20 to 40% by weight, based on the cumene, and cooling the reaction mixture to precipitate the α-naphthyl-N-methylcarbamate as a pure crystalline solid, the β-naphthyl-N-methylcarbamate formed in the reaction remaining in solution in the cumene when the reaction mixture is cooled.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04095034 |
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| Source dataset | uspto-grants-1978_06 |
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| ORD ID | ord-e72885e99d7640ed9e4782a98750c396 |
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| Source note | uspto-grants-1978_06 |
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