HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 22029155, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Benzyl 4-cyanopiperidine-1-carboxylate | HCID 22028286 | — |
| Reactant | HCID 67508035 | HCID 67508035 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 22029155 | HCID 22029155 | — |
Reaction Steps
Acetyl chloride (180 mL) was dropwise added to a mixture of ethanol (160 mL) and chloroform (180 mL) under ice-cooling. After the mixture was stirred for 30 min, a solution of 1-benzyloxycarbonyl-4-cyanopiperidine [product of Example 298 (2), 20.6 g] in chloroform (180 mL) was added thereto under ice-cooling. The mixture was stirred at room temperature for 18 hr. The reaction mixture was concentrated under reduced pressure to give 1-benzyloxycarbonyl-4-(ethoxycarbonimidoyl)piperidine hydrochloride (28.7 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07060722B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-45e9858145a147bf86da19d5a4123db0 |
| Source note | uspto-grants-2006_06 |