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

4-Chloro-N-(1,1-dimethyl-2-propynyl)benzamide → 2-(4-Chlorophenyl)-4,5-dihydro-4,4-dimethyl-5-methyleneoxazole

HRID 1107059
노트
인쇄 미리보기

반응식

HRID 1107059 반응식
[CH3:1][C:2]([NH:6][C:7](=[O:15])[C:8]1[CH:13]=[CH:12][C:11]([Cl:14])=[CH:10][CH:9]=1)([CH3:5])[C:3]#[CH:4]>[Cu]Cl.C(OCCCC)(=O)C>[Cl:14][C:11]1[CH:12]=[CH:13][C:8]([C:7]2[O:15][C:3](=[CH2:4])[C:2]([CH3:1])([CH3:5])[N:6]=2)=[CH:9][CH:10]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 327384-Chloro-N-(1,1-dimethyl-2-propynyl)benzamide

생성물 1

HCID 108678552-(4-Chlorophenyl)-4,5-dihydro-4,4-dimethyl-5-methyleneoxazole수율 100.2%

시약·촉매·용매 2

HCID 62652Cuprous chloride촉매HCID 31272Butyl Acetate용매

반응 조건

온도
95 °C

실험 절차

A round bottom flask was charged with N-(3-methylbutyn-3-yl)-4-chlorobenzamide (4.5 g, 19.09 mmol), copper(I) chloride (9.5 mg, 0.5 mol %), and n-butyl acetate (20 mL). The resulting mixture was heated to 95° C. for 4 h, then cooled to room temperature. The reaction was washed with 1 M hydrochloric acid solution and with water. The organic layer was dried over anhydrous sodium sulfate. The solvent was removed by evaporation under reduced pressure, and the residue was dried in a vacuum oven to afford 2-(4-chlorophenyl)-4,4-dimethyl-5-methyleneoxazoline (4.24 g, 94% yield) as a pale yellow oil (bp 95° C., 0.6 mm Hg).

후처리

  1. temperaturecooled to room temperature
  2. washThe reaction was washed with 1 M hydrochloric acid solution and with water
  3. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  4. customThe solvent was removed by evaporation under reduced pressure
  5. customthe residue was dried in a vacuum oven

출처 및 근거

ORD 기록
ord-c58de19889f94a969e34a18c6c4e3933
출처 데이터셋
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06057477

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트