Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499603Generated: November 2, 2026

Triphenylphosphine → HCID 86726822, compound

https://huagongshe.com/reaction/1499603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiphenylphosphoryl azideHCID 123414—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
ReactantHCID 86726819HCID 86726819—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86726822HCID 8672682286.5%

Reaction Steps

To a solution of tert-butyl (4R)-4-((1R,2S)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-cyclopropyl-3-hydroxypropyl)-2,2-dimethyl-1,3-oxazolidine-3-carboxylate (1.3 g, 3.0 mmol) and triphenylphosphine (1.6 g, 6.1 mmol) in anhydrous THF (20 mL), DIAD (1.2 mL, 5.9 mmol) was added drop-wise under an atmosphere of nitrogen. Upon completion of addition, a precipitate was formed. The reaction mixture was stirred for 30 min. then diphenylphosphonic azide (1.3 mL, 6.2 mmol) in anhydrous THF (1.0 mL) was added. After stirring at ambient temperature for 3 h, the volatile organic solvents were removed under reduced pressure and the crude product was purified by flash column chromatography (120 g of silica gel, eluting with 0-15% EtOAc-hexanes) to afford the sub-title compound as a light yellow oil (1.18 g, 86%). LC/MS (ESI) m/z calc. for C17H35N4O2Si: 355.30 [M-Boc+H]+. found: 355.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09200004B2
Source datasetuspto-grants-2015_12
ORD IDord-bf3dc55b43e7447fa655cef86f6b0b9a
Source noteuspto-grants-2015_12