HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 3-(1-Cyanocyclopropyl)benzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-(1-Cyanocyclopropyl)benzoic acid | HCID 57441039 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(1-Cyanocyclopropyl)benzoyl chloride | HCID 86631982 | — |
Reaction Steps
To a solution of 3-(1-cyanocyclopropyl)benzoic acid (139 mg, 0.742 mmol) produced in Example B3(ii) in tetrahydrofuran (7.0 mL) were added oxalyl chloride (80 μL, 0.929 mmol) and N,N-dimethylformamide (about 20 μL), and the mixture was stirred at room temperature for 1 hr. The reaction mixture was concentrated under reduced pressure to give 3-(1-cyanocyclopropyl)benzoyl chloride as a pale-brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08344135B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-93a3e83951064ed68cfe44a5e4996f65 |
| Source note | uspto-grants-2013_01 |