HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,8-Diazabicyclo(5.4.0)undec-7-ene → 4-(2-Cyanovinyl)-4-cyclohexylpiperidine-1-carboxylic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Dimethyl phosphono acetonitrile | HCID 20250566 | — |
| Reactant | 4-Cyclohexyl-4-formylpiperidine-1-carboxylic acid tert-butyl ester | HCID 21936875 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(2-Cyanovinyl)-4-cyclohexylpiperidine-1-carboxylic acid tert-butyl ester | HCID 69597086 | — |
Reaction Steps
To a solution of dimethyl phosphono acetonitrile (0.78 mL, 4.02 mmol), LiCl (184 mg, 4.02 mmol), and DBU (0.55 mL, 4.02 mmol) in anhydrous acetonitrile (25 mL) is added 4-cyclohexyl-4-formylpiperidine-1-carboxylic acid tert-butyl ester, 7, (992 mg, 3.35 mmol) under an atmosphere of argon at room temperature. The mixture is stirred for 1 hour and the solvent removed in vacuo. The resulting crude product is purified over silica gel eluting with dichloromethane/methanol 15:1 to afford the desired product in quantitative yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07026335B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-1a82d21f30c24478afcca70c9e47fd61 |
| Source note | uspto-grants-2006_04 |