HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazoethane → HCID 19757987, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazoethane | HCID 70695 | — |
| Reactant | 1-Azabicyclo(2.2.2)octane-3-carbonitrile | HCID 142865 | — |
| Reactant | HCID 19758000 | HCID 19758000 | — |
| Product | HCID 19757987 | HCID 19757987 | — |
Reaction Steps
This compound was prepared from (±) 3-cyano-1-azabicyclo[2.2.2]octane (EP-A-0 261 763, Description 1) in a similar manner to the compound of Example 2 using an ethereal solution of diazoethane prepared from N-nitroso-N-ethyl urea1,2. The resulting oil was purified by column chromatography using neutral alumina and eluting with 2% MeOH/EtOAc. 1H NMR indicated that the mixture contained a 12:1 ratio of the 2-ethyl isomer to 1-ethyl isomer and this mixture (100 mg, 17%) was crystallised and the title compound E9 recrystallised from methanol/diethyl ether as the oxalate salt (containing 8% of the 1-ethyl isomer).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05217975 |
| Source dataset | uspto-grants-1993_06 |
| ORD ID | ord-6e44745b98294840bdcabe5c34a48ce3 |
| Source note | uspto-grants-1993_06 |