HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 68881866, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 3-Bromobenzaldehyde | HCID 76583 | — |
| Reactant | 4-Mesylphenylacetic acid | HCID 572345 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 68881866 | HCID 68881866 | — |
Reaction Steps
Aryl Bromide AB1 was prepared by the following procedure. To a solution of 3-bromobenzaldehyde (12.9 g, 70 mmol) in toluene (100 mL) was added 4-(methylsulfonyl)phenylacetic acid (15 g, 70 mmol) and piperidine (2 mL). After overnight refluxing, the mixture was cooled down to r.t. To the slurry thus formed, toluene was added (10 mL). Filtration gave (E)-3-(3-Bromophenyl)-2-[4-(methylsulfonyl)phenyl]-2-propenoic acid as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06410563B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-f9de0470266c4cc283b591fd3d5b5f74 |
| Source note | uspto-grants-2002_06 |