HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 2-Cyano-4'-methylbiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 4'-Methyl[1,1'-biphenyl]-2-carbaldehyde | HCID 1394009 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-Cyano-4'-methylbiphenyl | HCID 145512 | 79% |
Reaction Steps
A mixture of 4′-methyl-2-biphenylcarbaldehyde (2.0 g) and hydroxyamine hydrochloride (1.0 g) in pyridine (10 ml) was stirred at room temperature for 15 min., followed by addition of acetic anhydride (4.1 g). The reaction mixture was stirred at 90-100° C. for 1 hr. and concentrated to dryness. After addition of water to the residue, the precipitated crystals were collected by filtration. Recrystallization from hexane gave colorless needles (1.5 g, 79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06608210B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-dab76be06e8a421e83c6062745357b02 |
| Source note | uspto-grants-2003_08 |