HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → N-(2-chloro-3-hydroxybenzyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2-Chloro-3-hydroxybenzaldehyde | HCID 593376 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(2-chloro-3-hydroxybenzyl)piperidine | HCID 21294597 | — |
Reaction Steps
In a similar manner to that described in Example 17 2-chloro-3-hydroxybenzaldehyde (9 g) in absolute ethanol (60 ml) was treated with piperidine (11.7 ml) and sodium borohydride (2.2 g) to yield N-(2-chloro-3-hydroxybenzyl)piperidine. The piperidine thus prepared was reacted with 4-bromobutyronitrile to give 4-(2-chloro-3-piperidinomethylphenoxy)butyronitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04767769 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-a40479b1925649b88b9ca5b70f57c52c |
| Source note | uspto-grants-1988_08 |