HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride etherate → HCID 178513157, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | HCID 46856402 | HCID 46856402 | — |
| Reactant | HCID 178418668 | HCID 178418668 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178513157 | HCID 178513157 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
To a screw cap pressure vessel was added the intermediate from Step A (3.22 g, 10.2 mmol), aminoguanidine hydrochloride (1.69 g, 15.3 mmol), methanol (25 mL) and boron trifluoride diethyl etherate (2.6 mL, 20.4 mmol). The reaction solution was heated at 100° C. for 70 minutes. The solution was concentrated and the residue partitioned between EtOAc and aqueous 1N NaOH. The organic phase was washed twice with aqueous 1N NaOH and brine (1×). The organic phase was dried over anhydrous magnesium sulfate, filtered and concentrated to give the indicated compound as a mixture of E, Z hydrazone isomers. 1H NMR (400 MHz, CD3CN): δ 7.54 (d, J=8.4 Hz, 1H); 7.24-7.17 (m, 1H); 7.10 (d, J=2.6 Hz, 1H); 2.68-2.51 (m, 4H). m/z 371 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365574B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-7858ae0047254cf0abba4fbc57cea805 |
| Source note | uspto-grants-2016_06 |