HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → HCID 13281349, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 4-(3-Chloro[1,1'-biphenyl]-2-yl)butanoic acid | HCID 13281348 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 13281349 | HCID 13281349 | — |
Reaction Steps
Under a dry argon atmosphere a stirred solution of 4-(3-chloro[1,1'-biphenyl]-2-yl)butanoic acid (22.8 g, 0.083 mole) in toluene (500 ml) was heated at 65°. Oxalyl chloride (21 g, 0.166 mole) was added slowly to the reaction mixture. After complete addition the mixture was allowed to stir at 40° for approximately 18 hours. The solvent and excess oxalyl chloride were removed by distillation under reduced pressure. Further distillation under reduced pressure gave 4-(3-chloro[1,1'-biphenyl]-2-yl)butanoic acid chloride (b.p. 150°/0.04 mm) as a clear oil. The nmr spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04507317 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-2e7a9bfc10f74ec4b684c42ed16fbaf9 |
| Source note | uspto-grants-1985_03 |