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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454628Generated: October 29, 2026

Triphenylphosphine → HCID 58508535, compound

https://huagongshe.com/reaction/454628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
ReactantHCID 58508682HCID 58508682—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58508535HCID 5850853513.8%

Reaction Steps

1-(tert-Butoxycarbonyl)-4-hydroxypiperidine (0.15 g), triphenylphosphine (0.21 g), and diisopropyl azodicarboxylate (0.16 mL) were added to a tetrahydrofuran (3.6 mL) suspension of methyl 2-(2,4-dihydroxybenzamido)-4-phenylbenzoate (0.24 g), followed by stirring at room temperature for 1 hour. 1-(tert-Butoxycarbonyl)-4-hydroxypiperidine (0.066 g), triphenylphosphine (0.086 g), and diisopropyl azodicarboxylate (0.064 mL) were added to the reaction mixture, followed by stirring at room temperature for 1 hour. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography [eluent: 100-75% hexane/ethyl acetate] to obtain 0.050 g of tert-butyl 4-(3-hydroxy-4-(2-(methoxycarbonyl)-5-phenylphenylcarbamoyl)phenoxy)piperidine-1-carboxylate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-bc500e0c86ba4372abb17f70a64db124
Source noteuspto-grants-2013_07