HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Cyanide → HCID 21023772, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Tosylmethyl isocyanide | HCID 161915 | — |
| Reactant | HCID 21023777 | HCID 21023777 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21023772 | HCID 21023772 | 42% |
Reaction Steps
A solution of 4-cyclohexyl-4-(3-oxo-propyl)-piperidine-1-carboxylic acid tert-butyl ester, 10, (300 mg, 0.93) in ethanol (10 ml) is treated with tosylmethyl isocyanide (tosMIC) (176 mg, 0.93 mmole) and sodium cyanide (6 mg) at room temperature for three hours. The solvent is removed under reduced pressure and ammonia in methanol (2M, 10 ml) added. The mixture is stirred in a sealed tube overnight. The reaction mixture is then concentrated under reduced pressure and the residue taken up in chloroform, washed with aqueous sodium bicarbonate, brine, then dried with sodium sulfate and concentrated to a red oil. The residue is purified over silica (methylene chloride:methanol=15:1, Rf=0.58) to afford 141 mg (42% yield) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07026335B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-ccdd26bae6114da5aa40a2155169759f |
| Source note | uspto-grants-2006_04 |