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

Tetrahydrofuran → Ethyl 4-(2,4-dichlorophenyl)-2,4-dioxobutanoate

HRID 1166174
노트
인쇄 미리보기

반응식

HRID 1166174 반응식
[CH3:1][C:2]([C:4]1[CH:9]=[CH:8][C:7]([Cl:10])=[CH:6][C:5]=1[Cl:11])=[O:3].C([N-]C(C)C)(C)C.[Li+].[C:20]([O:23][CH2:24][C:25](Cl)=[O:26])(=O)[CH3:21].C1C[O:31]CC1>>[Cl:11][C:5]1[CH:6]=[C:7]([Cl:10])[CH:8]=[CH:9][C:4]=1[C:2](=[O:3])[CH2:1][C:25](=[O:26])[C:24]([O:23][CH2:20][CH3:21])=[O:31]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 8028TetrahydrofuranHCID 166932',4'-DichloroacetophenoneHCID 26297Acetoxyacetyl chlorideHCID 2724682Lithium diisopropylamide

생성물 1

HCID 22997478Ethyl 4-(2,4-dichlorophenyl)-2,4-dioxobutanoate

반응 조건

온도
-78 °C

실험 절차

A solution of 2,4-dichloroacetophenone (3.78 g) in THF (20 ml) was cooled to −78° C. under a nitrogen atmosphere. To this stirred solution was added lithium diisopropylamide (LDA) (1.0 M, 22 ml) and the resulting solution was stirred at −78° C. for 15 minutes. Acetoxyacetyl chloride (2.3 ml) was injected and the mixture was stirred for 1 hour and then allowed to warm to room temperature. The reaction was quenched with 1N HCl and the product was extracted with diethyl ether (200 ml). The organic layer was dried, concentrated and recrystallized from ether/hexanes, yielding ethyl 4-(2,4-dichlorophenyl)-2,4-diketobutyrate (intermediate 1).

후처리

  1. stirringthe mixture was stirred for 1 hour
  2. temperatureto warm to room temperature
  3. customThe reaction was quenched with 1N HCl
  4. extractionthe product was extracted with diethyl ether (200 ml)
  5. customThe organic layer was dried
  6. concentrationconcentrated
  7. customrecrystallized from ether/hexanes

출처 및 근거

ORD 기록
ord-c18014cf62e6472a80820d149fbcfe83
출처 데이터셋
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06613777B1

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트