HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-(4-Cyano-cyclohexyl)-aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Tosylmethyl isocyanide | HCID 161915 | — |
| Reactant | 4-(4-Aminophenyl)cyclohexan-1-one | HCID 23371894 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 4-(4-Cyano-cyclohexyl)-aniline | HCID 23371869 | 56% |
Reaction Steps
392 mg (3.5 mmol) of potassium t-butylate were added portionwise at -10° to a suspension of 278 mg (1.5 mmol) of 4-(4-oxo-cyclohexyl)-aniline and 370 mg (1.9 mmol) of toluene-4-sulfonylmethylisocyanide in 5 ml of 1,2-dimethoxyethane and 0.15 ml of ethanol. After stirring at -5° for 1 hour and at room temperature for a further 70 hours 25 ml of water and 10 ml of saturated sodium chloride solution were added and the mixture was extracted three times with 40 ml of dichloromethane each time. The organic phase was dried with sodium sulfate and concentrated. Chormatography over silica gel with ethyl acetate/hexane 1:2 gave 165 mg (56%) of 4-(4-cyano-cyclohexyl)-aniline with m.p. 132°-140°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05574055 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-eac76925a80c4474b63b144e45559c3a |
| Source note | uspto-grants-1996_11 |