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

Phosphorus oxychloride → 2-(4-Trifluoromethylphenyl)-4-chloromethyl-5-methyloxazole

HRID 479130
노트
인쇄 미리보기

반응식

HRID 479130 반응식
[CH3:1][C:2]1[N+:3]([O-])=[C:4]([C:8]2[CH:13]=[CH:12][C:11]([C:14]([F:17])([F:16])[F:15])=[CH:10][CH:9]=2)[O:5][C:6]=1[CH3:7].O=P(Cl)(Cl)[Cl:21]>C(Cl)Cl>[Cl:21][CH2:1][C:2]1[N:3]=[C:4]([C:8]2[CH:13]=[CH:12][C:11]([C:14]([F:17])([F:16])[F:15])=[CH:10][CH:9]=2)[O:5][C:6]=1[CH3:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 10515280Oxazole, 4,5-dimethyl-2-[4-(trifluoromethyl)phenyl]-, 3-oxide

생성물 1

HCID 102363332-(4-Trifluoromethylphenyl)-4-chloromethyl-5-methyloxazole

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

18.5 g of the above prepared 4,5-dimethyl-2-(4-trifluoromethyl-phenyl)-oxazole 3-oxide (72 mmol) was dissolved in 250 ml of CH2Cl2 and treated with 7.909 ml of POCl3 (86.4 mmol). The reaction mixture was refluxed over night and then quenched by carefully pouring onto crashed ice/3N NaOH. Separation of the layers, additional extraction of the aqueous phase with CH2Cl2 and drying of the combined organic layers over magnesium sulfate left, after evaporation of the solvents, 19.78 g of crude product as light brown crystals, which was used as such for the next step.

후처리

  1. temperatureThe reaction mixture was refluxed over night
  2. customquenched
  3. additionby carefully pouring
  4. customSeparation of the layers, additional extraction of the aqueous phase with CH2Cl2
  5. dry with materialdrying of the combined organic layers over magnesium sulfate
  6. waitleft
  7. customafter evaporation of the solvents, 19.78 g of crude product as light brown crystals, which

출처 및 근거

ORD 기록
ord-9db056811bf64bd0867c42733b82fe7e
출처 데이터셋
uspto-grants-2003_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06642389B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트