Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064498Generated: November 1, 2026

Triphenylphosphine → Di-tert-butyl 1-(cyclopropylmethyl)hydrazine-1,2-dicarboxylate

https://huagongshe.com/reaction/2064498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantCyclopropanemethanolHCID 75644—
ReactantDi-tert-butyl bicarbamateHCID 85431—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
SolventTetrahydrofuranHCID 8028—
ProductDi-tert-butyl 1-(cyclopropylmethyl)hydrazine-1,2-dicarboxylateHCID 66643119354.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288428B2
Source datasetuspto-grants-2012_10
ORD IDord-77ab10bee8a34641b762f8c41cb5f93f
Source noteuspto-grants-2012_10