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

Chlorosuccinimide → 4-Chloro-N-hydroxybenzimidoyl chloride

HRID 1911654
노트
인쇄 미리보기

반응식

HRID 1911654 반응식
FC1C=CC(C=O)=CC=1.[Cl:10][C:11]1[CH:19]=[CH:18][C:14](/[CH:15]=[N:16]\[OH:17])=[CH:13][CH:12]=1.[Cl:20]N1C(=O)CCC1=O>CN(C=O)C>[OH:17]/[N:16]=[C:15](\[Cl:20])/[C:14]1[CH:18]=[CH:19][C:11]([Cl:10])=[CH:12][CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 31398ChlorosuccinimideHCID 87630081(NZ)-N-[(4-chlorophenyl)methylidene]hydroxylamine;4-fluorobenzaldehyde

생성물 1

HCID 72718654-Chloro-N-hydroxybenzimidoyl chloride수율 86.4%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a solution of (E)- and/or (Z)-4-chloro-benzaldehyde oxime 4-fluorobenzaldehyde (27.0 g, 173 mmol) in DMF (173 mL) was added N-chlorosuccinimide (22.8 g, 173 mmol) portionwise over 1 h, keeping the temperature below 35° C. The reaction mixture was stirred at room temperature for 1 h. The mixture was then poured onto ice-water, and extracted with ethyl acetate. The combined organic layers were then washed with water and brine, dried over sodium sulfate and evaporated to afford the title compound (28.4 g, 86%) which was obtained as a light yellow solid. MS: m/e=189.1 [M]+.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. customthe temperature below 35° C
  2. additionThe mixture was then poured onto ice-water
  3. extractionextracted with ethyl acetate
  4. washThe combined organic layers were then washed with water and brine
  5. dry with materialdried over sodium sulfate
  6. customevaporated

출처 및 근거

ORD 기록
ord-89e21046a7b846fd8e5313bbbe87caa2
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08604062B2

반응 노트

불러오는 중…