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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905975Generated: October 29, 2026

Triphenylphosphine → cis 2-[3-(Tert-butyl-dimethyl-silanyloxy)-cyclopentyl]-5,6-dichloro-isoindole-1,3-dione

https://huagongshe.com/reaction/905975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant4,5-DichlorophthalimideHCID 251543—
ReactantCyclopentanol, 3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, trans-HCID 58715064—
Solvent2-MethyltetrahydrofuranHCID 7301—
Productcis 2-[3-(Tert-butyl-dimethyl-silanyloxy)-cyclopentyl]-5,6-dichloro-isoindole-1,3-dioneHCID 86642299—

Reaction Steps

To a round bottomed flask was added trans 3-(tert-butyl-dimethyl-silanyloxy)-cyclopentanol (1.0 g, 4.62 mmol, prepared from WO2008065021), triphenylphosphine (1.52 g, 5.76 mmol) and 2-methyltetrahydrofuran (120 mL). Diisopropyl azodicarboxylate (1.23 mL, 6.25 mmol) was added over two minutes via syringe followed by 4,5-dichlorophthalimide (1.35 g, 6.25 mmol). The reaction was stirred overnight and evaporated. The reaction was repeated and the combined material was purified by column chromatography (160 g SiO2, EtOAc in hexane) to give cis 2-[3-(tert-butyl-dimethyl-silanyloxy)-cyclopentyl]-5,6-dichloro-isoindole-1,3-dione, a yellowish solid (2.0 gm, 52% yield)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012974B2
Source datasetuspto-grants-2011_09
ORD IDord-58f9c3e7181241a1a66dcc60ef94072b
Source noteuspto-grants-2011_09