HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyl phosphonoacetate → 4-Cyclohexyl-4-(2-methoxycarbonyl-vinyl)-piperidine-1-carboxylic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyl phosphonoacetate | HCID 80029 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 1,8-Diazabicyclo[4.3.0]non-7-ene | HCID 15788991 | — |
| Reactant | 4-Cyclohexyl-4-formylpiperidine-1-carboxylic acid tert-butyl ester | HCID 21936875 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Cyclohexyl-4-(2-methoxycarbonyl-vinyl)-piperidine-1-carboxylic acid tert-butyl ester | HCID 69597110 | 86% |
Reaction Steps
To a solution of trimethyl phosphonoacetate (1.41 ml, 8.72 mmole), lithium chloride (477 mg, 11.3 mmole), and 1,8-diazabicyclo[4.3.0]non-7-ene (DBU) (1.55 ml, 11.3 mmole) in anhydrous acetonitrile (25 ml) is added 4-cyclohexyl-4-formyl-piperidine-1-carboxylic acid tert-butyl ester, 7, (2.58 mg, 8.72 mmole) under argon at room temperature. The mixture is stirred for one hour and the solvent then removed under reduced pressure. The crude product is purified over silica (methylene chloride:methanol=15:1, Rf=0.78) to afford 2.64 g (86% yield) of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07026335B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-94b6c078e4e946cab61a484cb6848c8b |
| Source note | uspto-grants-2006_04 |