홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Sodium Hydroxide → ethyl 4-bromo-5-ethyl-1H-pyrrole-2-carboxylate

HRID 2233813
노트
인쇄 미리보기

반응식

HRID 2233813 반응식
[Br:1]N1C(=O)CCC1=O.[CH2:9]([C:11]1[NH:15][C:14]([C:16]([O:18][CH2:19][CH3:20])=[O:17])=[CH:13][CH:12]=1)[CH3:10].[OH-].[Na+]>C(Cl)Cl>[Br:1][C:12]1[CH:13]=[C:14]([C:16]([O:18][CH2:19][CH3:20])=[O:17])[NH:15][C:11]=1[CH2:9][CH3:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 67184N-bromobutanimideHCID 597485Ethyl 5-ethyl-1H-pyrrole-2-carboxylate2회

생성물 1

HCID 68580112ethyl 4-bromo-5-ethyl-1H-pyrrole-2-carboxylate수율 68%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

N-Bromosuccinimide (5.86 g, 0.033 mol) was added to a solution of ethyl 5-ethyl-1H-pyrrole-2-carboxylate (Intermediate 12, 5.0 g, 0.03 mol) in DCM (85 ml) at 0° C., and the reaction was stirred for 30 minutes then poured to a chilled beaker containing 2 N NaOH (50 ml). The layers were separated and the aqueous layer was extracted with DCM (×3). The combined organic extracts were washed with water and brine, dried over magnesium sulfate and concentrated. The resultant dark brown solid was purified by flash chromatography (hexanes/EtOAc, 10:1) to give the title product as a white solid (5.0 g, 68%).

후처리

  1. additionthen poured to a chilled beaker
  2. customThe layers were separated
  3. extractionthe aqueous layer was extracted with DCM (×3)
  4. washThe combined organic extracts were washed with water and brine
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated
  7. customThe resultant dark brown solid was purified by flash chromatography (hexanes/EtOAc, 10:1)

출처 및 근거

ORD 기록
ord-e135598ffb5446758f60c3f60b9e7749
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07709503B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트