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

Carbon tetrabromide → 5-bromomethyl-1-(2,6-dichlorophenyl)-4-trifluoromethyl-1H-triazole

HRID 424823
노트
인쇄 미리보기

반응식

HRID 424823 반응식
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Cl:20][C:21]1[CH:26]=[CH:25][CH:24]=[C:23]([Cl:27])[C:22]=1[N:28]1[C:32]([CH2:33]O)=[C:31]([C:35]([F:38])([F:37])[F:36])[N:30]=[N:29]1.C(Br)(Br)(Br)[Br:40]>ClCCl>[Br:40][CH2:33][C:32]1[N:28]([C:22]2[C:21]([Cl:20])=[CH:26][CH:25]=[CH:24][C:23]=2[Cl:27])[N:29]=[N:30][C:31]=1[C:35]([F:38])([F:37])[F:36]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11205Carbon tetrabromideHCID 11776TriphenylphosphineHCID 66704107[3-(2,6-Dichloro-phenyl)-5-trifluoromethyl-3H-[1,2,3]triazol-4-yl]methanol

생성물 1

HCID 866292535-bromomethyl-1-(2,6-dichlorophenyl)-4-trifluoromethyl-1H-triazole수율 99.8%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
0 °C

실험 절차

Triphenylphosphine (16.4 g, 62.5 mmol) is added to a suspension of [3-(2,6-dichlorophenyl)-5-trifluoromethyl-3H-[1,2,3]triazol-4-yl]-methanol (13 g, 41.69 mmol) in dichlormethane (80 mL). The mixture is cooled to 0° C. and carbon tetrabromide (20.7 g, 62.5 mmol) is added. The reaction is stirred at room temperature for 1.5 hours. The solvent is evaporated under reduced pressure and the residue is purified by flash chromatography eluting with hexanes/EtOAc (95:5 to 8:2) to obtain the title compound (15.6 g, 96% yield). ES/MS m/e 374 (M+1).

후처리

  1. customThe solvent is evaporated under reduced pressure
  2. customthe residue is purified by flash chromatography
  3. washeluting with hexanes/EtOAc (95:5 to 8:2)

출처 및 근거

ORD 기록
ord-c0597f6422ea4552934eb46de0b78687
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08106077B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트