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

4-acetyl-5-methyl-2-phenyloxazole N-oxide hydrochloride → 1-(5-Methyl-2-phenyl-1,3-oxazol-4-yl)ethan-1-one

HRID 487745
노트
인쇄 미리보기

반응식

HRID 487745 반응식
Cl.[C:2]([C:5]1[N+:6]([O-])=[C:7]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[O:8][C:9]=1[CH3:10])(=[O:4])[CH3:3]>C(O)(=O)C.[Zn]>[C:2]([C:5]1[N:6]=[C:7]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[O:8][C:9]=1[CH3:10])(=[O:4])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 190930604-acetyl-5-methyl-2-phenyloxazole N-oxide hydrochloride

생성물 1

HCID 123378491-(5-Methyl-2-phenyl-1,3-oxazol-4-yl)ethan-1-one수율 12.6%

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 176Acetic Acid용매

실험 절차

Next, 100 g of 4-acetyl-5-methyl-2-phenyloxazole N-oxide hydrochloride was dissolved in 500 ml of glacial acetic acid and 100 g of zinc powder was added to the solution while cool stirring within a ice water bath. The separation was filtered after addition of 2 l of water and recrystalization was carried out by addition of methanol to produce 10 g of 4-acetyl-5-methyl-2-phenyloxazole (melting point; 74° to 76° C.).

후처리

  1. temperaturewhile cool
  2. customThe separation
  3. filtrationwas filtered
  4. additionafter addition of 2 l of water and recrystalization
  5. additionwas carried out by addition of methanol

출처 및 근거

ORD 기록
ord-22b2523d82a0402698f11211b08c1e18
출처 데이터셋
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05296607

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트