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

Water → 2-Phenyl-4-(2,6-difluorophenyl)oxazole

HRID 1738380
노트
인쇄 미리보기

반응식

HRID 1738380 반응식
[F:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]([F:12])[C:3]=1[C:4](=O)[CH2:5]Br.[C:13]([NH2:21])(=[O:20])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.O>CC1C=CC=CC=1C>[C:14]1([C:13]2[O:20][CH:5]=[C:4]([C:3]3[C:2]([F:1])=[CH:11][CH:10]=[CH:9][C:8]=3[F:12])[N:21]=2)[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 2331BenzamideHCID 27782632,6-Difluorophenacyl bromide

생성물 1

HCID 217155952-Phenyl-4-(2,6-difluorophenyl)oxazole수율 121.8%

시약·촉매·용매 1

HCID 7237O-Xylene용매

실험 절차

5.7 g 2,6-difluorophenacyl bromide and 3.63 g benzamide were suspended in 20 ml o-xylene, and the suspension was subjected to reflux under heating for 1.5 hours. After completing the reaction, the suspension reacted was added with water, then extracted with ethyl acetate and further washed with saturated saline solution. The organic layer obtained was dried with anhydrous magnesium sulfate, and the solvent used was removed by distillation under reduced pressure. Out of 7.6 g residue obtained, 1.0 g thereof was purified by using silica gel column chromatography, affording the objective substance in an amount of 0.6 g.

후처리

  1. temperatureto reflux
  2. temperatureunder heating for 1.5 hours
  3. customthe reaction
  4. customthe suspension reacted
  5. extractionextracted with ethyl acetate
  6. washfurther washed with saturated saline solution
  7. customThe organic layer obtained
  8. dry with materialwas dried with anhydrous magnesium sulfate
  9. customthe solvent used was removed by distillation under reduced pressure

출처 및 근거

ORD 기록
ord-0924e2a4ac5e421595e2eb83470635df
출처 데이터셋
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05962685

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트