Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1,3,3,5,5-Pentamethylcyclohexanol | HCID 142288 | — |
| Product | HCID 18783143 | HCID 18783143 | 60% |
Reaction Steps
To a vigorously stirred solution of 1,3,3,5,5-pentamethylcyclohexanol (3-13) (3.0 g, 17.65 mmol) in acetonitrile (20 ml) fuming HNO3 (6ml) was added dropwise, keeping temperature below 45° C. The resulting mixture was stirred at -50° C. for 6 h, then it was cooled, poured into water (30 ml) ana neutralised with aqueous NH3. Aqueous phase was extracted with ether (3*30 ml). The combined ether phases were washed with saline (30 ml), then dried over MgSO4, filtered and evaporated. The crude product was crystallised from cold acetonitrile to give 223 g (60%) of 14-2 as a white crystals, m.p. 110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06071966 |
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| Source dataset | uspto-grants-2000_06 |
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| ORD ID | ord-11ed142ceef94d2e99b3f55577bf2078 |
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| Source note | uspto-grants-2000_06 |
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