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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042447Generated: October 31, 2026

Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester → 3-(2-Propylamino-4-trifluoromethyl-phenyl)-acrylic acid methyl ester

https://huagongshe.com/reaction/1042447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic acid, 2-(triphenylphosphoranylidene)-, methyl esterHCID 17453—
Reactant2-Propylamino-4-trifluoromethyl-benzaldehydeHCID 86649955—
SolventTolueneHCID 1140—
Product3-(2-Propylamino-4-trifluoromethyl-phenyl)-acrylic acid methyl esterHCID 6685551169%

Reaction Steps

N-Methoxy-N-methyl-2-propylamino-4-trifluoromethyl-benzamide (98.3 mg, 0.339 mmol) was reacted with 1M lithium aluminum hydride (0.6 ml) in THF (20 ml) at −40° C. for 1 hr. The reaction mixture was quenched by adding saturated potassium hydrogen sulfate solution. The mixture was stirred for 30 min. The reactions solvent was removed in vacuo. Water (30 ml) was added to the resulting residue, which was extracted with CH2Cl2 (30 ml×3). The combined organic layer was dried over MgSO4 and concentrated in vacuo to yield 2-propylamino-4-trifluoromethyl-benzaldehyde (78 mg). 2-Propylamino-4-trifluoromethyl-benzaldehyde in toluene was reacted with methyl (triphenylphosphoranylidene) acetate (137 mg) at 100° C. overnight. The reaction solvent was removed in vacuo. Water (30 ml) was added to the resulting residue, which was extracted with ethyl acetate (30 ml×3). The combined organic layer was dried over MgSO4 and filtered. The filterate was concentrated in vacuo and purified with column chromatography to yield title compound (67 mg, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557872B2
Source datasetuspto-grants-2013_10
ORD IDord-1c192df185334e51889354a6eb57f9fa
Source noteuspto-grants-2013_10