HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromobutyronitrile → 4-(2-Chloro-3-piperidinomethylphenoxy)butyronitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromobutyronitrile | HCID 21412 | — |
| Reactant | N-(2-chloro-3-hydroxybenzyl)piperidine | HCID 21294597 | — |
| Product | 4-(2-Chloro-3-piperidinomethylphenoxy)butyronitrile | HCID 21294553 | — |
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-83f7587f3fc4437aabe7bd529e5d8791 |
| Source note | uspto-grants-1988_08 |