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

carbazic acid, dithio-, monopotassium salt → Ethyl 5-sulfanyl-1,3,4-thiadiazole-2-carboxylate

HRID 1988203
노트
인쇄 미리보기

반응식

HRID 1988203 반응식
[CH2:1]([O:3][C:4](=[O:9])[C:5](SC)=S)[CH3:2].[NH:10]([C:12]([S-:14])=[S:13])[NH2:11].[K+]>C(O)C>[SH:13][C:12]1[S:14][C:5]([C:4]([O:3][CH2:1][CH3:2])=[O:9])=[N:11][N:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10909709carbazic acid, dithio-, monopotassium saltHCID 12427868Ethyl (methylsulfanyl)(sulfanylidene)acetate

생성물 1

HCID 178470473Ethyl 5-sulfanyl-1,3,4-thiadiazole-2-carboxylate

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Ethyl(methylthio)(thioxo)acetate (20.0 g, 122 mmol) and potassium hydrazinecarbodithioate (R. S. Drago et al., JACS (1983) 105, 2287) (17.8 g, 122 mmol) were reflux overnight in ethanol (500 ml). The solution was concentrated and EtOAc was added. The organic phase was washed with 1M HCl, brine and dried over anhydrous Na2SO4. The solvent was evaporated and the residue purified on silica gel (hexanes-acetone, 80:20) to give the title compound. 1H NMR (400 MHz, acetone-d6): 4.43 (q, 2H), 1.38 (t, 3H).

후처리

  1. concentrationThe solution was concentrated
  2. additionEtOAc was added
  3. washThe organic phase was washed with 1M HCl, brine
  4. dry with materialdried over anhydrous Na2SO4
  5. customThe solvent was evaporated
  6. customthe residue purified on silica gel (hexanes-acetone, 80:20)

출처 및 근거

ORD 기록
ord-46f267bc728043b4ad6218c483c21f94
출처 데이터셋
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07553973B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트