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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523463Generated: November 3, 2026

Triphenylphosphine → (R)-tert-butyl 4-((1R,2S)-3-azido-1-(tert-butyldimethylsilyloxy)-2-methylpropyl)-2,2-dimethyloxazolidine-3-carboxylate

https://huagongshe.com/reaction/1523463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactant(R)-tert-butyl 4-((1R,2S)-1-(tert-butyldimethylsilyloxy)-3-hydroxy-2-methylpropyl)-2,2-dimethyloxazolidine-3-carboxylateHCID 59226545—
SolventTetrahydrofuranHCID 8028—
Product(R)-tert-butyl 4-((1R,2S)-3-azido-1-(tert-butyldimethylsilyloxy)-2-methylpropyl)-2,2-dimethyloxazolidine-3-carboxylateHCID 5922647986%

Reaction Steps

To a solution of (R)-tert-butyl 4-((1R,2S)-1-(tert-butyldimethyl-silyloxy)-3-hydroxy-2-methylpropyl)-2,2-dimethyloxazolidine-3-carboxylate (1.0 equiv.), DIAD (2.0 equiv.), and PPh3 (2.0 equiv.) in THF (0.18 M) was added DPPA (2.0 equiv., 1M solution in THF). The reaction mixture was stirred at room temperature overnight. Upon removal of the volatiles under vacuo, the residue was purified by silica gel column chromatography eluting with ethyl acetate and hexanes (1:6) to give (R)-tert-butyl 4-((1R,2S)-3-azido-1-(tert-butyldimethylsilyloxy)-2-methylpropyl)-2,2-dimethyloxazolidine-3-carboxylate as the major product (5:2) in 86% yield. LC/MS=329.3 (M+H-Boc), Rt=1.40 min (Frac 65%-95% method).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079889B2
Source datasetuspto-grants-2015_07
ORD IDord-2c2829a38c924187ad9abb93a2ad9333
Source noteuspto-grants-2015_07