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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171752Generated: November 2, 2026

Ammonium Chloride → HCID 23138815, compound

https://huagongshe.com/reaction/1171752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 23139093HCID 23139093—
SolventEthanolHCID 702—
ProductHCID 23138815HCID 23138815101.6%

Reaction Steps

To a solution of (E)-3-{[1-(ethoxycarbonylmethyl)-1H-pyrazol-4-yl]methylidene}-1-(triphenylmethyl)piperidin-4-one (6.08 g) in ethanol (100 ml) was added sodium borohydride (230 mg). The resulting mixture was stirred at room temperature for 30 minutes, and the reaction was stopped by addition of a saturated aqueous ammonium chloride solution. The products were extracted with ethyl acetate, and the organic layer was washed with a saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was evaporated in vacuo to afford the title compound as a yellow amorphous solid (6.2 g, yield: quantitative).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829580B2
Source datasetuspto-grants-2010_11
ORD IDord-4e0147270fa44fa493a5e48aa74f66c8
Source noteuspto-grants-2010_11