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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042483Generated: October 30, 2026

Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester → 3-(4-Fluoro-2-propylamino-phenyl)-acrylic acid methyl ester

https://huagongshe.com/reaction/1042483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic acid, 2-(triphenylphosphoranylidene)-, methyl esterHCID 17453—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 86649966HCID 86649966—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product3-(4-Fluoro-2-propylamino-phenyl)-acrylic acid methyl esterHCID 6685642870.8%

Reaction Conditions

Temperature-35 °C

Reaction Steps

To a solution of N-methoxy-N-methyl-4-fluoro-2-propylamino-benzamide (0.33 g, 1.37 mmol) in THF (4 mL) was added dropwise LiAlH4 (1 M in THF, 0.7 mL) at −45° C. The mixture was stirred for 40 minutes at −35° C. and then quenched by adding saturated aqueous KHSO4 solution. The mixture was diluted with EtOAc, washed with 3 N HCl, and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The resulting residue was reacted with methyl (triphenylphosphoranylidene)acetate (0.5 g, 1.5 mmol) in toluene (4 mL) overnight at 100° C. The mixture was washed with water, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to give the title compound (0.23 g, 69%) after purification by column chromatography (EtOAc:hexane=1:10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557872B2
Source datasetuspto-grants-2013_10
ORD IDord-354b6e60db4b4814b8e31d0feb235318
Source noteuspto-grants-2013_10