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HRID 641811作成日:2026年10月27日

Sodium Carbonate → 2,5-Dimethyl-1-phenyl-3-vinyl-1H-pyrrole

https://huagongshe.com/reaction/641811

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物2,5-Dimethyl-1-phenylpyrrole-3-carboxaldehydeHCID 66515—
反応物Phosphonium, (bromomethyl)triphenyl-, bromide (1:1)HCID 2733422—
触媒Tetrabutylammonium ChlorideHCID 70681—
触媒palladium(II) acetateHCID 167845—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物2,5-Dimethyl-1-phenyl-3-vinyl-1H-pyrroleHCID 5925928880%

反応手順

To a solution of bromomethyl(triphenyl)phosphonium bromide (2.2 g, 5 mmol) in dry THF (50 mL), n-Bu.Li (2.5 M, 2 mL, 5 mmol) was added dropwise at −78° C. under nitrogen. The reaction mixture was stirred 30 min at this temperature and compound 5 (1.0 g, 5 mmol) was added, then the cooling bath was removed. Stirring was continued for another hour. The solvent was completely removed under reduced pressure. The residue and Pd(OAc)2 (56 mg, 0.25 mmol), Na2CO3 (1.86 g, 17.5 mmol), n-Bu4NCl (8.34 g, 30 mmol) were dissolved in dried DMF (20 mL). The reaction mixture was stirred at 100° C. for 3 hrs. The reaction was quenched by adding 20 mL of water, and the aqueous phase was extracted with EtOAc (30 mL×3). The combined extracts were dried over Na2SO4, the mixture was filtered and the filtrate was concentrated in vacuo to give the desired product as a colorless oil (Purity: 90%, yield: 80%). MS [M++1]=198, LC-MS: tR=2.76 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07696227B2
出典データセットuspto-grants-2010_04
ORD IDord-ed8a1fa325284775801e048133aced16
出典メモuspto-grants-2010_04