HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dinitrobenzonitrile → HCID 66745849, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dinitrobenzonitrile | HCID 520718 | — |
| Reactant | (Oxan-4-yl)methanol | HCID 2773573 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 66745849 | HCID 66745849 | 83.2% |
Reaction Steps
To a solution of tetrahydropyran-4-methanol (782 mg, 6.73 mmol) in THF (25 mL), was added slowly 1.38M nBuLi (4.13 mL, 5.70 mmol) in hexane at −78° C. under nitrogen. At one hour a solution of 2,6-dinitrobenzonitrile (1.00 g, 5.18 mmol) in THF (25 mL) was added. The reaction was stirred under N2 overnight at rt, then was quenched with water (100 mL). The precipitate was collected by filtration to provide 2-nitro-6-((tetrahydro-2H-pyran-4-yl)methoxy)benzonitrile (1.13 g, 83%) as a light brown solid. 1H NMR (400 MHz, DMSO-d6) δ 1.68 (m, 2H), 2.06 (br, 1H), 3.33 (m, 2H), 3.88 (m, 2H), 4.11 (d, J=6.0 Hz, 2H), 7.72 (d, J=6.0 Hz, 1H), 7.89-7.85 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08633186B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-8e846e88adcf4de2979c5465bafba585 |
| Source note | uspto-grants-2014_01 |