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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620112Generated: November 1, 2026

Triphenylphosphine → (2S)-2-((tert-butoxycarbonyl)amino)hexane-3-yl 4-nitrobenzoate

https://huagongshe.com/reaction/1620112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant4-NitrobenzoateHCID 4419940—
Reactanttert-butyl((2S)-3-hydroxyhexan-2-yl)carbamateHCID 87514848—
SolventTetrahydrofuranHCID 8028—
Product(2S)-2-((tert-butoxycarbonyl)amino)hexane-3-yl 4-nitrobenzoateHCID 8668388159.3%

Reaction Steps

4-nitrobenzoate (16.3 g), triphenylphosphine (32 g), and diisopropyl azodicarboxylate (40% toluene solution) (64 ml) were added dropwise to a tetrahydrofuran (50 ml) solution containing tert-butyl((2S)-3-hydroxyhexan-2-yl)carbamate (17 g) for 30 minutes, followed by stirring at room temperature for 14 hours. The solvent was distilled away from the reaction solution under reduced pressure, the obtained residue was purified by silica gel chromatography (n-hexane:ethyl acetate=5.5:1), and a yellow solid of (2S)-2-((tert-butoxycarbonyl)amino)hexane-3-yl 4-nitrobenzoate (17 g) was thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772320B2
Source datasetuspto-grants-2014_07
ORD IDord-93705581dad54b999f56bb2df6dc3551
Source noteuspto-grants-2014_07