HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → tert-Butyl 2-(4-fluorobenzoyl)hydrazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-Fluorobenzoic Acid | HCID 9973 | — |
| Reactant | tert-Butyl carbazate | HCID 70091 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl 2-(4-fluorobenzoyl)hydrazine-1-carboxylate | HCID 67279032 | — |
Reaction Steps
To a solution of 4-fluorobenzoic acid (35.7 mmol) in 72 mL of a mixture of DMF and THF (1:1), is added tert-butyl carbazate (37.5 mmol), EDC (39.3 mmol) and N,N-dimethylaminopyridine (0.54 mmol). After 10 minutes the mixture becomes homogeneous and stirring is continued for 3 hours until the reaction is complete by TLC and LC/MS. The reaction mixture is poured into ice. Upon addition of diethylether the organic layer is separated. The organic layer is washed with sodium bisulfite, saturated sodium bicarbonate and saturated sodium chloride solution, dried over magnesium sulfate and concentrated to yield N′-(4-fluoro-benzoyl)-hydrazinecarboxylic acid tert-butyl ester: MS: (ES+) 255 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08569345B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-ac2523e226fc441484b99a8acb011207 |
| Source note | uspto-grants-2013_10 |