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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17875Generated: October 25, 2026

Triphenylphosphine → 1-oxo-3-phenyl-6-(3-phenylpropoxy)-1H-indene-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/17875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantBenzenepropanolHCID 31234—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant6-hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acid ethyl esterHCID 11845279—
SolventTetrahydrofuranHCID 8028—
Product1-oxo-3-phenyl-6-(3-phenylpropoxy)-1H-indene-2-carboxylic acid ethyl esterHCID 1184528285%

Reaction Steps

6-Hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylate ethyl ester (1.7 g, 6.07 mmol), 3-phenylpropanol (1.65 g, 12.14 mmol) and triphenylphosphine (3.18 g, 12.14 mmol) were dissolved in tetrahydrofuran (100 ml). Diethyl azodicarboxylate (2 ml, 12.14 mmol) dissolved in tetrahydrofuran (20 ml) was added dropwise thereto at 0° C. After stirring for 6 hours at room temperature, the mixture was washed with brine, extracted with ethyl acetate, the extract was dried over anhydrous magnesium sulfate, the concentrated under a reduced pressure, and the residue was purified by silica gel column chromatography (diethyl ether:hexane=1:10) to obtain the title compound (yield 85%) as a dark red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741323B2
Source datasetuspto-grants-2010_06
ORD IDord-b01a65d8d7f7470f9c3b2f407b55bba8
Source noteuspto-grants-2010_06