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HRID 1642352생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1642352

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2,5-Dimethyl-1-phenylpyrrole-3-carboxaldehydeHCID 66515—
반응물Phosphonium, (bromomethyl)triphenyl-, bromide (1:1)HCID 2733422—
반응물ButyllithiumHCID 178418339—
촉매Tetrabutylammonium ChlorideHCID 70681—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물2,5-Dimethyl-1-phenyl-3-vinyl-1H-pyrroleHCID 5925928880%

반응 단계

To a solution of bromomethyl(triphenyl)phosphonium bromide (2.2 g, 5 mmol) in dry THF (50 mL), n-BuLi (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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08119660B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-937e390fabe04d86bfa76d6a93f5785f
출처 메모uspto-grants-2012_02