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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant1,1-Dimethylethyl octahydro-5-hydroxy-2H-isoindole-2-carboxylateHCID 18670324—
SolventDichloromethaneHCID 6344—
Product2-Boc-5-oxo-octahydro-isoindoleHCID 1867045786.8%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518423B1
Source datasetuspto-grants-2003_02
ORD IDord-4a5ed146f509423cb0807849304716f4
Source noteuspto-grants-2003_02