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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751510Generated: November 1, 2026

Triphenylphosphine → HCID 69270257, compound

https://huagongshe.com/reaction/751510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant5-HydroxyindoleHCID 16054—
Reactant2-(Tert-butoxy)ethan-1-olHCID 24232—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 69270257HCID 6927025736.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

Add triphenylphosphine (600 mg, 2.29 mmol) to a solution of diethyl azodicarboxylate (0.36 mL, 2.29 mmol) in methylene chloride (10 ml) at 0° C. followed by ethylene glycol mono-t-butyl ether (0.30 mL, 2.29 mmol), and stir the mixture for 20 minutes at 0° C. Add 5-hydroxyindole (200 mg, 1.5 mmol), remove the cold bath, and stir for 5 hours. Add water (2 mL), transfer the resultant mixture to a separatory funnel, and separate the layers. Wash the organic layer with 0.1 N aqueous HCl and brine, then dry over sodium sulfate, filter, and concentrate. Purification by flash chromatography and eluting with hexane:ethyl acetate gives 127 mg (36%) of the title compound as a light yellow solid. Mass spectrum: electrospray (m/z) 232 (M−−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405305B2
Source datasetuspto-grants-2008_07
ORD IDord-b54e96a5228846e6aaeb7cfc317a1324
Source noteuspto-grants-2008_07