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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406760Generated: November 1, 2026

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

https://huagongshe.com/reaction/2406760

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 numberUS08809371B2
Source datasetuspto-grants-2014_08
ORD IDord-90ffe9cbe28643a4b6e1c6f5d8c39e64
Source noteuspto-grants-2014_08