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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203327Generated: November 2, 2026

Boron trifluoride etherate → HCID 178513156, compound

https://huagongshe.com/reaction/2203327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
Reactant1-(2-Bromo-5-chlorophenyl)-4,4,5,5,5-pentafluoropentan-1-oneHCID 86678967—
ReactantHCID 178418668HCID 178418668—
SolventMethanolHCID 887—
ProductHCID 178513156HCID 178513156—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a screw cap pressure vessel was added the intermediate from Step B (0.450 g, 1.2 mmol), aminoguanidine hydrochloride (0.456 g, 6.2 mmol), methanol (20 mL) and boron trifluoride diethyl etherate (0.94 mL, 7.4 mmol). The reaction solution was heated at 100° C. for 3 hours. 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 hyrazone isomers. 1H NMR (500 MHz, CH3OH-d4): δ 7.60 (d, J=8.6 Hz, 1H); 7.26-7.23 (m, 1H); 7.18 (d, J=2.5 Hz, 1H); 2.74 (s, 2H); 2.56 (s, 2H). m/z=421.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365574B2
Source datasetuspto-grants-2016_06
ORD IDord-04af3ed8111f40aa97bd75802e5ce216
Source noteuspto-grants-2016_06