HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246740Generated: November 1, 2026
Triphenylphosphine → HCID 68523774, compound
https://huagongshe.com/reaction/2246740
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 3,3-Dimethyl-1,3-dihydro-indol-2-one | HCID 313100 | — |
| Reactant | (S)-(-)-3-Chloro-1-phenyl-1-propanol | HCID 2777894 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68523774 | HCID 68523774 | 34.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07687529B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-191b7f30b2924bdfa310f8ab19ed8c27 |
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| Source note | uspto-grants-2010_03 |
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