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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171667Generated: November 1, 2026

Ammonium Chloride → HCID 23138758, compound

https://huagongshe.com/reaction/1171667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 23138559HCID 23138559—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 23138758HCID 23138758102.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

(E)-3-({1-[2-(Methoxycarbonyl)ethyl]-1H-1,2,3-triazol-5-yl}methylidene)-1-(triphenylmethyl)piperidin-4-one (12.87 g) was dissolved in a mixed solvent of dichloromethane (100 ml) and methanol (100 ml). While the solution was being stirred at 0° C., sodium borohydride (480 mg) was added thereto. The resulting mixture was stirred at 0° C. for 30 minutes, and the reaction was stopped by addition of a saturated aqueous ammonium chloride solution. The product was extracted with dichloromethane. The organic layer was washed with a saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure to afford the crude title compound (13.22 g) as a pale yellow amorphous solid. This product was used in the next process without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829580B2
Source datasetuspto-grants-2010_11
ORD IDord-331311e9c071454cac1146602f627bf1
Source noteuspto-grants-2010_11