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

Isopropyl iodide → 5-chloro-2-isopropoxybenzaldehyde

HRID 1728164
노트
인쇄 미리보기

반응식

HRID 1728164 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([OH:10])=[C:6]([CH:9]=1)[CH:7]=[O:8].I[CH:12]([CH3:14])[CH3:13].C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:10][CH:12]([CH3:14])[CH3:13])=[C:6]([CH:9]=1)[CH:7]=[O:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6362Isopropyl iodideHCID 11430Potassium CarbonateHCID 124815-Chloro-salicylaldehyde

생성물 1

HCID 51996155-chloro-2-isopropoxybenzaldehyde수율 78.8%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

5-Chloro-2-hydroxy-benzaldehyde (3 g, 19.16 mmol),2-Iodo-propane (4.88 g, 28.74 mmol) and K2CO3 (4 g, 28.74 mmol) was mixed in anhydrous DMF. The reaction tube was placed into the cavity of a focused monomode microwave reactor and the contents of the flask were irradiated for 30 min at 100° C. Then the solution was filtered and the filtration was concentrated to obtain the crude product (3 g). The crude product was used into next step reaction without further purification.

후처리

  1. customThe reaction tube was placed into the cavity of a focused monomode microwave reactor
  2. customthe contents of the flask were irradiated for 30 min at 100° C
  3. filtrationThen the solution was filtered
  4. filtrationthe filtration
  5. concentrationwas concentrated

출처 및 근거

ORD 기록
ord-831fe5f47a49478886682d089bd99e2a
출처 데이터셋
uspto-grants-2009_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07495007B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트