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

Water → HCID 338434, 화합물

HRID 478334
노트
인쇄 미리보기

반응식

HRID 478334 반응식
[CH3:1][C:2]1[C:3]([CH2:13]O)=[N:4][N:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:6]=1.S(Cl)([Cl:17])=O.O.C(=O)([O-])[O-].[K+].[K+]>ClCCl>[Cl:17][CH2:13][C:3]1[C:2]([CH3:1])=[N:6][N:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 24386Thionyl ChlorideHCID 563195(5-Methyl-2-phenyl-2H-1,2,3-triazol-4-yl)methanol

생성물 1

HCID 338434HCID 338434, 화합물수율 94.8%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

5.0 g of (5-methyl-2-phenyl-1,2,3-triazol4-yl)methan-1-ol was dissolved in 35 ml of dichloromethane, then 6.3 g of thionyl chloride was added dropwise thereto under cooling with ice. After stirring for 1 hour at room temperature, 100 ml of water was added. The resulting solution was made alkaline with 8 g of potassium carbonate, then extracted with chloroform. The organic phase was washed with water and a saturated salt solution, then dried over anhydrous sodium sulfate. After the solvent was distilled off, 5.2 g of the aimed compound was obtained.

후처리

  1. temperatureunder cooling with ice
  2. extractionextracted with chloroform
  3. washThe organic phase was washed with water
  4. dry with materiala saturated salt solution, then dried over anhydrous sodium sulfate
  5. distillationAfter the solvent was distilled off

출처 및 근거

ORD 기록
ord-731a40a655e04c39ad33a8669a41bb40
출처 데이터셋
uspto-grants-2003_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06642234B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트