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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester | HCID 17453 | — |
| Reactant | 2-Propylamino-4-trifluoromethyl-benzaldehyde | HCID 86649955 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-(2-Propylamino-4-trifluoromethyl-phenyl)-acrylic acid methyl ester | HCID 66855511 | 69% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08557872B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-1c192df185334e51889354a6eb57f9fa |
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| Source note | uspto-grants-2013_10 |
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