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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21382Generated: October 29, 2026

Ammonium Chloride → HCID 15639108, compound

https://huagongshe.com/reaction/21382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant8-Benzylidene-9-azatricyclo[4.3.1.04,9]decan-7-oneHCID 54362685—
ReactantHCID 178418255HCID 178418255—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 15639108HCID 1563910853%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 100 ml three-necked round-bottomed flask equipped with a rubber septum and nitrogen inlet were added 5 ml dry toluene and 4.43 ml (13.3 mmol) of a 3.0M solution of phenyl magnesium bromide in ether. The solution was cooled to 0° C., and a solution of 2.07 g (8.87 mmol) 8-benzylidene-9-azatricyclo[4.3.1.04,9 ]decan-7-one in 20 ml toluene was added over 5 min. The reaction was allowed to stir at 0° C. for 1 hour and then poured into saturated aqueous ammonium chloride. The mixture was extracted into ethyl acetate, and the organic layer washed with saturated aqueous ammonium chloride and brine, dried over sodium sulfate, and evaporated. The residue was chromatographed on silica gel using hexane/ethyl acetate as eluent and the product fractions combined to afford 1.47 g (53%) of a white solid, mp 137°-138° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05422354
Source datasetuspto-grants-1995_06
ORD IDord-bf51c633bf9d4bd1adbf8f55f53dad27
Source noteuspto-grants-1995_06