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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177771Generated: November 2, 2026

Ammonium Chloride → HCID 58864516, compound

https://huagongshe.com/reaction/1177771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant5-Hydroxy-2-nitrobenzaldehydeHCID 39211—
Reactant1-Benzyl-4-piperidylamineHCID 415852—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
ProductHCID 58864516HCID 5886451657%

Reaction Steps

5-Hydroxy-2-nitro-benzaldehyde (5 g, 29.9 mmol) and 4-amino-1-benzylpiperidine (5.6 mL, 29.9 mmol) were combined in ethanol (30 mL). The resulting suspension was stirred at room temperature for 20 min before a solution of sodium borohydride (1.13 g, 29.9 mmol) in ethanol (10 mL) was added dropwise over 10 min. After the addition was complete, the reaction was stirred at room temperature for 1 h, cooled to 0° C. and concentrated ammonium chloride added to the reaction mixture until no bubbling was observed. The solvents were evaporated in vacuo and the resultant crude mixture was dissolved in water (30 mL) and methylene chloride (40 mL). The layers were separated and the organic layer washed with water (2×), brine (2×), dried over sodium sulfate, filtered, and concentrated to afford 5.8 g (57%) of the desired product. LC/MS: tR=0.95 min, 342.27 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842808B2
Source datasetuspto-grants-2010_11
ORD IDord-3e0d9bd67abc443eaa95c9865789c3a2
Source noteuspto-grants-2010_11