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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384906Generated: October 26, 2026

Triphenylphosphine → Rac-[1-(4-chloro-phenyl)-2-oxo-2-[4-(tetrahydro-pyran-3-yloxy)-phenyl]-ethyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/384906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
Reactanttetrahydro-2H-pyran-3-olHCID 12256033—
ReactantRac-[1-(4-chloro-phenyl)-2-(4-hydroxy-phenyl)-2-oxo-ethyl]-carbamic acid tert-butyl esterHCID 68409176—
SolventTetrahydrofuranHCID 8028—
ProductRac-[1-(4-chloro-phenyl)-2-oxo-2-[4-(tetrahydro-pyran-3-yloxy)-phenyl]-ethyl]-carbamic acid tert-butyl esterHCID 68408312—

Reaction Steps

To a solution of 250 mg (0.691 mmol) rac-[1-(4-chloro-phenyl)-2-(4-hydroxy-phenyl)-2-oxo-ethyl]-carbamic acid tert-butyl ester, 257 mg (0.864 mmol) triphenylphosphine and 84.7 mg (0.829 mmol) tetrahydro-pyran-3-ol in 8.5 ml tetrahydrofuran were added 191 mg (0.829 mmol) di-tert-butyl azodicarboxylate and the reaction mixture stirred at ambient temperature for 2 hours. Then the reaction mixture was evaporated and purified by flash chromatography on silica gel with a heptane/ethyl acetate gradient of 0-30% ethyl acetate. The title compound was obtained as colorless solid: MS (ISN): 444.2 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367838B2
Source datasetuspto-grants-2013_02
ORD IDord-40c154a8db834e39b99fb8cea1c54de0
Source noteuspto-grants-2013_02