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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480245Generated: October 31, 2026

(NE)-N-(2,2-dimethylpropylidene)-2-methylpropane-2-sulfinamide → HCID 90204274, compound

https://huagongshe.com/reaction/1480245

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(NE)-N-(2,2-dimethylpropylidene)-2-methylpropane-2-sulfinamideHCID 11506602—
Reactant2-Bromo-5-methyl-1,3,4-oxadiazoleHCID 25219536—
ReactantHCID 178418918HCID 178418918—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 90204274HCID 9020427464%

Reaction Conditions

Temperature-15 °C

Reaction Steps

To a solution of 2-bromo-5-methyl-1,3,4-oxadiazole (CAN 864750-58-3, 0.473 g, 2.91 mmol) in dry THF (8 ml) cooled down to −15° C. under an argon atmosphere was added isopropyl magnesium chloride, lithium chloride complex (2.23 ml, 2.91 mmol). (During the addition the temperature was kept below −12° C.). The reaction was then stirred at −15° C. for 30 minutes followed by slow addition of a solution of (NE)-N-(2,2-dimethylpropylidene)-2-methyl-propane-2-sulfinamide (CAN 917104-90-6, 500 mg, 2.64 mmol) in dry toluene (8 ml). The reaction was allowed to warm up to room temperature overnight. The reaction was quenched by addition of water. The reaction medium was diluted with ethylacetate and the organic phase was extracted with a saturated aqueous solution of ammonium chloride. The organic phase was collected and the aqueous phase was back-extracted with ethylacetate. The combined organic phases were dried over sodium sulfate and evaporated down to dryness. The crude material was purified by flash chromatography on silica eluting with a dichloromethane/methanol gradient to yield the title compound (462 mg, 64%). MS (ESI, m/z): 274.5 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409866B2
Source datasetuspto-grants-2016_08
ORD IDord-5a5f5b25921e488aa6bdb5e8e5125bf3
Source noteuspto-grants-2016_08