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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1800824Generated: November 2, 2026

Dimethyl Sulfoxide → HCID 59321452, compound

https://huagongshe.com/reaction/1800824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantCarbonate IonHCID 19660—
ReactantBenzeneacetonitrile, 2,3-dichloro-HCID 229020—
ReactantN-BOC-N,N-Bis(2-chloroethyl)amineHCID 11230235—
SolventEthyl AcetateHCID 8857—
ProductHCID 59321452HCID 5932145258.9%

Reaction Steps

2-(2,3-dichlorophenyl)acetonitrile (2.49 g crude, est. 83% purity, 11 mmol), 2.70 g tert-butyl bis(2-chloroethyl)carbamate (J. Med. Chem. 1992, 35, 11, 2033-2039) (11 mmol), 19.5 g aesium carbonate (60 mmol) and 200 ml DMSO were combined in a round bottom flask and stirred at room temperature for 4 days. The reaction mixture was diluted with ethyl acetate and the organic layer washed with 1M aq. KHSO4 solution, and then saturated aq. NaHCO3 solution, then brine. The organic layer was dried over magnesium sulfate, filtered and concentrated. The product was purified by column chromatography on silica, using a gradient from 5% to 35% ethyl acetate in hexanes as eluent. 2.3 g of the title compound were isolated as an oil (59% yield)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343999B2
Source datasetuspto-grants-2013_01
ORD IDord-ca44cc99ca3346389606882531aa7c25
Source noteuspto-grants-2013_01