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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171273Generated: November 1, 2026

Diiodomethane → HCID 89666888, compound

https://huagongshe.com/reaction/2171273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 89666886HCID 89666886—
ReactantHCID 178418750HCID 178418750—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 89666888HCID 89666888—

Reaction Steps

A methylene chloride (3 ml) solution containing diiodomethane (0.2 ml) and a methylene chloride solution (3 ml) containing 2-((1R,6S)-6-(benzyl ((R)-1-phenylethyl)amino)-3-cyclohexen-1-yl)isoindolin-1,3-dione (0.36 g) obtained in the 1st step were added to a methylene chloride solution (10 ml) containing diethyl zinc (1M in hexane) (2.47 ml), followed by stirring for 15 hours. Methanol and sodium hydrogen carbonate were added to the reaction solution. The reaction solution was filtered through Celite. The filtrate was extracted with ethyl acetate. The organic layers were washed with water and saturated saline and dried over anhydrous sodium sulfate. The solvent was distilled away under reduced pressure and the obtained residue was purified by silica gel chromatography (n-hexane:ethyl acetate=1:0 to 1:0.2). A 2-((3R,4S)-4-(benzyl ((R)-1-phenylethyl)amino)bicyclo[4.1.0]heptan-3-yl)isoindolin-1,3-dione (0.20 g) was thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051310B2
Source datasetuspto-grants-2015_06
ORD IDord-8cb9b2964ce7449b827a7327f5a81802
Source noteuspto-grants-2015_06