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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192548Generated: November 1, 2026

Ammonium Acetate → HCID 58368683, compound

https://huagongshe.com/reaction/1192548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 58368651HCID 58368651—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
ProductHCID 58368683HCID 58368683—

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 1-[4-chloro-1-(3-fluorophenyl)-2-naphthyl]ethanone (58 mg, 0.19 mmol) and ammonium acetate (150 mg, 1.94 mmol) in methanol (1.1 mL) and acetonitrile (1.1 mL) was heated at 65° C., in a sealed tube for 30 minutes. After cooling to room temperature, sodium cyanoborohydride (24.4 mg, 0.388 mmol) was added to the resulting mixture. The reaction was heated at 65° C. for another 4 hours, then cooled to room temperature and quenched with sat. sodium bicarbonate and extracted with dichloromethane. The combined extracts were dried over magnesium sulfate and evaporated to dryness. The crude material was used directly in the next step (58 mg, 100%). LCMS calculated for C18H13ClF (M−NH2)+: m/z=283.1; Found: 283.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680108B2
Source datasetuspto-grants-2014_03
ORD IDord-6a5b9e803e644521a955cad01d9271f9
Source noteuspto-grants-2014_03