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

Trityl chloride → (N-triphenylmethyltetrazol-5-yl]thiophene

HRID 1646075
노트
인쇄 미리보기

반응식

HRID 1646075 반응식
[C:1]([C:3]1[S:4][CH:5]=[CH:6][CH:7]=1)#[N:2].[Sn]([N:12]=[N+:13]=[N-:14])(C)(C)C.[C:15](Cl)([C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.CCN(CC)CC>C1(C)C=CC=CC=1.C(Cl)Cl.CCOCC.CCOC(C)=O>[C:16]1([C:15]([C:22]2[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=2)([C:28]2[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=2)[N:12]2[C:1]([C:3]3[S:4][CH:5]=[CH:6][CH:7]=3)=[N:2][N:14]=[N:13]2)[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 6456Trityl chlorideHCID 8471TriethylamineHCID 660872-ThiophenecarbonitrileHCID 5104973Azido(trimethyl)stannane

생성물 1

HCID 16637535(N-triphenylmethyltetrazol-5-yl]thiophene수율 80%

시약·촉매·용매 3

HCID 1140Toluene
용매
HCID 6344Dichloromethane용매
HCID 21584169Diethylether ethylacetate용매

실험 절차

To a solution of 2-cyanothiophene (1.4 g; 12.8 mmol) in dry toluene (10 ml) was added Me3SnN3 (2.8 g; 13.65 mmol). The mixture was stirred at reflux under N2 for 12 hours. The reaction was cooled to room temperature diluted with CH2Cl2 and washed with 2N HCl soln and H2O. The organic was dried over anhydrous MgSO4 and concentrated in vacuo. The residue, containing the free tetrazole, was dissolved in CH2Cl2 (10 mL) and Ph3CCl (3.2 g; 0.9 equiv.) and NEt3 (3.6 mL) were added. After 20 minutes the mixture was diluted with Et2O/EtOAc and washed with 1N NaOH, 10% citric acid and brine. The organic was dried over anhydrous MgSO4 and concentrated in vacuo. The product was purified by recrystallization from hexanes. The titled compound was isolated in 80% yield, Rf=0.33 (10:1 hex/EtOAc). 1H NMR (200 MHz, CDCl3) δ7.12-7.21 (comp, 8H), 7.28-7.40 (comp, 8H), 7.42 (dd, 1H), 7.79 (dd, 1H).

후처리

  1. temperatureat reflux under N2 for 12 hours
  2. washwashed with 2N HCl soln and H2O
  3. dry with materialThe organic was dried over anhydrous MgSO4
  4. concentrationconcentrated in vacuo
  5. additionThe residue, containing the free tetrazole
  6. dissolutionwas dissolved in CH2Cl2 (10 mL)
  7. washwashed with 1N NaOH, 10% citric acid and brine
  8. dry with materialThe organic was dried over anhydrous MgSO4
  9. concentrationconcentrated in vacuo
  10. customThe product was purified by recrystallization from hexanes

출처 및 근거

ORD 기록
ord-936378b0bac748a6a28f40e8fbb72937
출처 데이터셋
uspto-grants-1993_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05177074

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트