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

Triethylamine → ethyl 3-bromo-4-chloro-5-methyl-1H-pyrrole-2-carboxylate

HRID 655752
노트
인쇄 미리보기

반응식

HRID 655752 반응식
[Br:1]Br.[Cl:3][C:4]1[CH:5]=[C:6]([C:10]([O:12][CH2:13][CH3:14])=[O:11])[NH:7][C:8]=1[CH3:9].CCN(CC)CC.OS([O-])=O.[Na+]>C(Cl)Cl>[Br:1][C:5]1[C:4]([Cl:3])=[C:8]([CH3:9])[NH:7][C:6]=1[C:10]([O:12][CH2:13][CH3:14])=[O:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8471TriethylamineHCID 24408BromineHCID 23665763Sodium BisulfiteHCID 66707189ethyl 4-chloro-5-methyl-1H-pyrrole-2-carboxylate

생성물 1

HCID 66707680ethyl 3-bromo-4-chloro-5-methyl-1H-pyrrole-2-carboxylate수율 106.2%

시약·촉매·용매 1

HCID 6344
Dichloromethane
용매

실험 절차

Bromine (0.56 ml, 11 mmol) was added to a solution of 1 g (5.3 mmol) of ethyl 4-chloro-5-methyl-1H-pyrrole-2-carboxylate (WO2006087543) and 0.8 ml (5.7 mmol) Et3N in CH2Cl2. After stirring at room temperature for 2 h, aqueous NaHSO3 was added and the CH2Cl2 was removed and the aqueous residue was partitioned between water and EtOAc. The EtOAc layer was separated and washed with brine. The EtOAc layer was dried over anhydrous MgSO4, and the solvent was removed to give 1.5 g of the product as a solid. MS (ES) (MH+): 240 for C8H9BrClNO2; NMR (d6-DMSO): 1.3 (t, 3H), 2.2 (s, 3H), 4.2 (q, 2H), 12.3 (s, 1H).

후처리

  1. customthe CH2Cl2 was removed
  2. customthe aqueous residue was partitioned between water and EtOAc
  3. customThe EtOAc layer was separated
  4. washwashed with brine
  5. dry with materialThe EtOAc layer was dried over anhydrous MgSO4
  6. customthe solvent was removed

출처 및 근거

ORD 기록
ord-f8c919a1364e42e788a071f2188cd9ef
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08071605B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트