HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → Di-tert-butyl 1-(cyclopropylmethyl)hydrazine-1,2-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Cyclopropanemethanol | HCID 75644 | — |
| Reactant | Di-tert-butyl bicarbamate | HCID 85431 | — |
| Reactant | Di-tert-butyl azodicarboxylate | HCID 97268 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Di-tert-butyl 1-(cyclopropylmethyl)hydrazine-1,2-dicarboxylate | HCID 66643119 | 354.4% |
Reaction Steps
To a mixture of cyclopropylmethanol (7.15 ml, 90 mmol), di-tert-butyl hydrazine-1,2-dicarboxylate (6.30 g, 27.1 mmol) and triphenylphosphine (28.5 g, 109 mmol) in THF (100 mL) was added di-tert-butyl azodicarboxylate (25 g, 109 mmol) portion wise at ambient temperature. The mixture was stirred for 2 hours then concentrated. Solid triphenylphosphineoxide was removed by filtration. The filtrate was concentrated and the residue was purified by flash chromatography (silica gel, eluted with a gradient of 5-25% EtOAc in hexane) to provide 27.5 g (96%) of title compound. 1H NMR (300 MHz, CDCl3) δ ppm 0.15-0.26 (m, 2H), 0.42-0.54 (m, 2H), 0.91-1.09 (m, 1H), 1.47 (s, 9H), 1.48 (s, 9H), 3.31 (d, J=6.10 Hz, 2H), 6.38 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08288428B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-77ab10bee8a34641b762f8c41cb5f93f |
| Source note | uspto-grants-2012_10 |