HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → N-(2-chloro-5-hydroxybenzyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Chloro-5-hydroxybenzaldehyde | HCID 21294524 | — |
| Reactant | 4-(4-Chloro-3-piperidinomethylphenoxy)butyronitrile | HCID 21294569 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(2-chloro-5-hydroxybenzyl)piperidine | HCID 21294588 | — |
Reaction Steps
In a similar manner to that described in Example 17 4-(4-chloro-3-piperidinomethylphenoxy)butyronitrile was prepared by the reaction of 2-chloro-5-hydroxybenzaldehyde (1.379 g), piperidine (1.8 ml) and sodium borohydride (0.33 g) in absolute ethanol (10 ml) to produce N-(2-chloro-5-hydroxybenzyl)piperidine which was then reacted with 4-bromobutyronitrile to yield the above-mentioned product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04767769 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-95815a52177f4c3bb8ffeaa4ad63dff2 |
| Source note | uspto-grants-1988_08 |