Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867553Generated: October 30, 2026

Triphenylphosphine → HCID 67528786, compound

https://huagongshe.com/reaction/1867553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant2,4-OxazolidinedioneHCID 97389—
ReactantHCID 67528572HCID 67528572—
SolventAcetoneHCID 180—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67528786HCID 67528786112.6%

Reaction Steps

A solution of 1.0 g (4.20 mmol) of 2-[4-(1H-pyrrolo[2,3-b]pyridin-1-yl)phenyl]ethanol, prepared in step 13.1., 0.51 g (5.04 mmol) of 1,3-oxazolidine-2,4-dione and 1.21 g (4.62 mmol) of triphenylphosphine in 16 ml of tetrahydrofuran, cooled by a bath of acetone and ice, is admixed dropwise with 0.84 g (4.2 mmol) of diisopropyl azodicarboxylate in solution in 2 ml of tetrahydrofuran. The mixture is subsequently heated to ambient temperature again and stirred overnight. 4 g of silica are added and the mixture is evaporated to dryness. The residue is purified by chromatography on silica gel, eluting with a 70/30 then 60/40 then 50/50 and 40/60 mixture of cyclohexane and ethyl acetate, to give 1.52 g of product in the form of a sticky solid, which is used as it is in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632850B2
Source datasetuspto-grants-2009_12
ORD IDord-f0eb4adc32654774ab5ce5d00d12a18b
Source noteuspto-grants-2009_12