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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246740Generated: November 1, 2026

Triphenylphosphine → HCID 68523774, compound

https://huagongshe.com/reaction/2246740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant3,3-Dimethyl-1,3-dihydro-indol-2-oneHCID 313100—
Reactant(S)-(-)-3-Chloro-1-phenyl-1-propanolHCID 2777894—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68523774HCID 6852377434.2%

Reaction Steps

To a mixture of 3,3-dimethyloxindole (409 mg, 2.53 mmol), (S)-3-chloro-1-phenyl-1-propanol (376 mg, 2.20 mmol) and triphenylphosphine (664 mg, 2.53 mmol) in tetrahydrofuran (5 mL) under nitrogen was added slowly diisopropyl azodicarboxylate (490 μL, 2.53 mmol) via a syringe. The resulting solution was stirred at room temperature overnight. Solvent was removed under reduced pressure and the viscous brown liquid residue was purified using Isco CombiFlash Companion chromatography (RediSep 12-g silica column, 0-12% ethyl acetate/hexane) to give 236 mg (34%) of 1-[(1R)-3-chloro-1-phenylpropyl]-3,3-dimethyl-1,3-dihydro-2H-indol-2-one as a viscous colorless liquid. MS (ES) m/z 314.1 ([M+H]+); HRMS: calculated for C19H20ClNO+H+, 314.1306; found (ESI, [M+H]+), 314.1299.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687529B2
Source datasetuspto-grants-2010_03
ORD IDord-191b7f30b2924bdfa310f8ab19ed8c27
Source noteuspto-grants-2010_03