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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 644800생성일: 2026년 10월 26일

1-Bromo-3-methylbutane → Ethyl 1-isopentyl-4-nitro-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/644800

반응식

참여 물질

역할이름HCID투입량
반응물1-Bromo-3-methylbutaneHCID 7891—
반응물Ethyl 4-Nitropyrrole-2-carboxylateHCID 242169—
반응물PotassiumHCID 5462222—
용매DimethylformamideHCID 6228—
생성물Ethyl 1-isopentyl-4-nitro-1H-pyrrole-2-carboxylateHCID 6718332085.1%

반응 조건

온도100 °C

반응 단계

Ethyl 4-nitro-1H-pyrrole-2-carboxylate (2.022 g, 10.983 mmol; see Example 1, step (i) above) was dissolved in DMF (30 mL, dry) to which potassium (0.569 g, 14.552 mmol) was added with stirring under nitrogen. The reaction mixture was heated at 100° C. for 1 h and then the temperature was allowed to reach 50° C. Isoamyl bromide (2.498 g, 16.538 mmol) was then added, followed by KI (2.197 g, 14.552 mmol). The temperature was raised to 100° C. and stirring continued for 5 h, after which time the temperature was allowed to return to room temperature. The reaction mixture was then stirred overnight, following which the solvent was removed under reduced pressure at 50° C. The crude product was dissolved in DCM and the salt extracted with water. The organic extract was dried over MgSO4, filtered and the solvent removed under reduced pressure at 30° C. The crude product obtained was chromatographed over silica gel using 1/2 n-hexane/DCM as eluant. Material with Rf=0.3 was collected and the solvent was removed under reduced pressure to give white crystalline material (2.377 g, 85% yield). M.p. 46-47° C. (Lit. m.p. 46-47° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07700765B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-865a6b2724cd424aa18d4080505407b1
출처 메모uspto-grants-2010_04