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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402976Generated: October 31, 2026

Triethylamine → 2-Fluoro-5-((3-oxoisobenzofuran-1(3H)-ylidene)methyl)benzonitrile

https://huagongshe.com/reaction/1402976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Fluoro-5-formylbenzonitrileHCID 2769582—
ReactantDimethyl (3-oxo-1,3-dihydro-2-benzofuran-1-yl)phosphonateHCID 11118213—
SolventTetrahydrofuranHCID 8028—
Product2-Fluoro-5-((3-oxoisobenzofuran-1(3H)-ylidene)methyl)benzonitrileHCID 67122451—

Reaction Conditions

Temperature20 °C

Reaction Steps

To a mixture of (3-oxo-1,3-dihydro-isobenzofuran-1-yl)phosphonic acid dimethyl ester (35.0 g, 0.14 mol) in tetrahydrofuran (200 ml) and 2-fluoro-5-formylbenzonitrile (20.9 g, 0.14 mol) in tetrahydrofuran (130 ml) was added triethylamine (14 ml, 0.14 mol) drop-wise over 25 min, with the temperature kept below 15° C. The reaction mixture was warmed slowly to 20° C. over 1 hour and concentrated in vacuo. The white residue was slurried in water (250 ml) for 30 minutes, filtered, washed with water, hexane and ether, and dried to yield 2-fluoro-5-(3-oxo-3H-isobenzofuran-1-ylidenemethyl)benzonitrile as a 50:50 mixture of E and Z isomers (37.2 g, 96%); m/z [M+1]+ 266 (98% purity)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912187B2
Source datasetuspto-grants-2014_12
ORD IDord-c85db88245704be39004d179a4dfc86a
Source noteuspto-grants-2014_12