HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromophenylhydrazine hydrochloride → 4-(3-Bromophenyhydrazono)-1-butanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromophenylhydrazine hydrochloride | HCID 33757 | — |
| Reactant | 2,3-Dihydrofuran | HCID 70934 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(3-Bromophenyhydrazono)-1-butanol | HCID 67613181 | 99.6% |
Reaction Steps
Under anhydrous conditions a solution of 3-bromophenylhydrazine hydrochloride (22.5 g, 100 mmol) and 2,3-dihydrofuran (7.55 ml, 100 mmol) in 200 ml of dry THF was stirred at ambient temperature for 3 h. The reaction mixture was partitioned between EtOAc and H2O. The organic phase was washed with H2O and brine. After drying (Na2 SO4), the solvent was evaporated to give 25.6 g of the product as a brown oil. The product was of suitable purity for use in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05824699 |
| Source dataset | uspto-grants-1998_10 |
| ORD ID | ord-71f44accceb34da08c5f8b2e174c5c94 |
| Source note | uspto-grants-1998_10 |