HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Cyanophenylhydrazine Hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | N-(4-Cyano-phenyl)-hydrazinecarboxylic Acid tert-butyl Ester | HCID 11230036 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Cyanophenylhydrazine Hydrochloride | HCID 16212962 | — |
Reaction Steps
Title compound 52A, N-(4-cyano-phenyl)-hydrazinecarboxylic acid tert-butyl ester (0.23 g, 1.0 eq, 0.99 mmol) was suspended in a mixture of 4M HCl in Dioxane (4.2 ml, 17.0 eq, 16.8 mmol) and DCM (5 ml). The mixture was then stirred at room temperature for 18 hours The resultant precipitate was isolated by filtration and washed with DCM to yield the title compound as a cream solid. (0.14 g, 0.8 mmol, 85%). 1H NMR (DMSO) 400 MHz: Indicates product in >95% purity
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08071607B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-c859f5cb14dc4d8f84fc86e38cdd5bb9 |
| Source note | uspto-grants-2011_12 |