Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Menthol | HCID 1254 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 14639416 | HCID 14639416 | — |
Reaction Steps
1.9 g of 2,6-difluorobenzoylisocyanate were added to a solution of 2.47 g of 4-dl-menthyloxy-aniline in a mixture of 15 ml of diethyl ether and 15 ml of petroleum ether (60-80) while stirring at room temperature. After adding 35 ml of petroleum ether (60-80), stirring was continued for another hour, after which the formed prepcipitate was sucked off, washed with petroleum ether and dried. The desired product was obtained in a yield of 4.1 g; melting-point 189°-190° C. The starting aniline was obtained from the corresponding nitro compound by reduction with hydrogen under the influence of Raney nickel as a catalyst, ethyl acetate being used as a solvent. 1-Nitro-4-dl-menthyloxybenzene was prepared by reaction of dl-menthol with 1-fluoro-4-nitrobenzene in tert.-butanol as a solvent in the presence of potassium tert.-butoxide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04656193 |
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| Source dataset | uspto-grants-1987_04 |
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| ORD ID | ord-824df436b47d49d7ae370ff67769c344 |
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| Source note | uspto-grants-1987_04 |
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