HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716615Generated: October 30, 2026
Tert-Butyl nitrite → HCID 11294280, compound
https://huagongshe.com/reaction/1716615
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | HCID 11518638 | HCID 11518638 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11294280 | HCID 11294280 | 55.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07803832B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-5174c536bcf2413f88363a4730a815a8 |
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| Source note | uspto-grants-2010_09 |
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