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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716615Generated: October 30, 2026

Tert-Butyl nitrite → HCID 11294280, compound

https://huagongshe.com/reaction/1716615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-Butyl nitriteHCID 10906—
ReactantHCID 11518638HCID 11518638—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11294280HCID 1129428055.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of Example 20 (150 mg, 0.31 mmol) in tetrahydrofuran (5 ml) was added dropwise tert-butyl nitrite (111 μl, 0.93 mmol). The reaction mixture was then heated at 60° C. overnight. The reaction mixture was concentrated in vacuo and the residue was partitioned between ethyl acetate (20 ml) and water (20 ml). The organic layer was separated, washed with brine (20 ml), dried (Na2SO4) and concentrated in vacuo. The residue was purified by column chromatography (silica, 10 g) eluting with dichloromethane/ethyl acetate [9:1]. The appropriate fractions were combined and concentrated to give the crude product. The crude product was dissolved in a mixture of acetonitrile, dimethyl sulphoxide and water (4:5:1, 2 ml) and purified by automated preparative liquid chromatography (Gilson system, 150 mm×30 mm Phenomonex LUNA C18(2) 10 μm column) using an acetonitrile:water gradient [60:40 to 95:5]. The appropriate fractions were concentrated in vacuo to give the titled compound (80 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803832B2
Source datasetuspto-grants-2010_09
ORD IDord-5174c536bcf2413f88363a4730a815a8
Source noteuspto-grants-2010_09