HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059314Generated: November 1, 2026
Dimethyl Sulfoxide → 2-Boc-5-oxo-octahydro-isoindole
https://huagongshe.com/reaction/1059314
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 1,1-Dimethylethyl octahydro-5-hydroxy-2H-isoindole-2-carboxylate | HCID 18670324 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Boc-5-oxo-octahydro-isoindole | HCID 18670457 | 86.8% |
Reaction Steps
4.9 g of oxalyl chloride was dissolved in 250 ml of dichloromethane and cooled to −78° C. in a nitrogen atmosphere. Then a solution of 4.83 g of dimethyl sulfoxide in dichloromethane (20 ml) was dropped thereinto over 17 minutes. Subsequently, a solution of 3.73 g of 8-(tert-butoxycarbonyl)-8-azabicyclo[4.3.0]nonan-3-ol in dichloromethane (40 ml) was dropped thereinto over 10 minutes. After stirring for 10 minutes, 7.82 g of triethylamine was dropped thereinto over 10 minutes and stirring was continued for additional 1 hour. The reaction mixture was brought back to room temperature, diluted with dichloromethane, washed with water and a saturated aqueous solution of sodium chloride and then dried over anhydrous magnesium sulfate. After filtration, the solvent was distilled off under reduced pressure. The residue thus obtained was purified by silica gel column chromatography (eluted with n-hexane/ethyl acetate) to thereby give 3.21 g of the title compound as a colorless oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06518423B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-4a5ed146f509423cb0807849304716f4 |
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| Source note | uspto-grants-2003_02 |
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