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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191670Generated: October 31, 2026

Ammonium Chloride → HCID 69670903, compound

https://huagongshe.com/reaction/1191670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86665747HCID 86665747—
SolventEthanolHCID 702—
ProductHCID 69670903HCID 6967090376.8%

Reaction Steps

To a suspension of 1-benzenesulfonyl-5-formyl-2-phenylindole (224 mg) in ethanol (2.5 mL) was added sodium borohydride (11.7 mg), and the mixture was stirred at room temperature for one hour. A saturated aqueous ammonium chloride solution was added to the reaction mixture and the resulting mixture was extracted with ethyl acetate. The organic layer was washed with saturated saline, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluting solvent: ethyl acetate-hexane) to obtain the title compound (173 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680120B2
Source datasetuspto-grants-2014_03
ORD IDord-4a189ab9ee264ab8ad3369313a107619
Source noteuspto-grants-2014_03