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

Carbon Disulfide → HCID 12694981, 화합물

HRID 67967
노트
인쇄 미리보기

반응식

HRID 67967 반응식
[NH2:1][C@@H:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([Br:12])[CH:10]=2)[CH2:5][CH2:4][C@H:3]1[NH2:13].[C:14](=S)=[S:15]>C(O)C>[Br:12][C:9]1[CH:10]=[C:11]2[C:6]([CH2:5][CH2:4][C@H:3]3[NH:13][C:14](=[S:15])[NH:1][C@@H:2]32)=[CH:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6348Carbon DisulfideHCID 12694952Trans-1,2-diamino-7-bromo-1,2,3,4-tetrahydronaphthalene

생성물 1

HCID 12694981HCID 12694981, 화합물수율 70%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Trans-1,2-diamino-7-bromo-1,2,3,4-tetrahydronaphthalene (6.75 g, 28.0 m mol) was dissolved in ethanol (70 ml) and carbon disulfide (1.9 ml, 31.7 m mol) was added to the solution. After stirring at room temperature for 20 minutes, they were heated under reflux for 5.5 hours. The reaction mixture was cooled in an ice bath and crystals precipitated were collected by filtration, whereby trans-8-bromo-3a,4,5,9b-tetrahydronaphth[1,2-d]imidazoline-2-thione (5.57 g) was obtained in 70% yield. The crystals were recrystallized from methanol-acetonitrile to give pale-yellow crystals melting at 259.5°-260.5° C. (decomposition). The product gave the following data on spectroscopy and elemental analysis.

후처리

  1. temperaturethey were heated
  2. temperatureunder reflux for 5.5 hours
  3. temperatureThe reaction mixture was cooled in an ice bath
  4. customcrystals precipitated
  5. filtrationwere collected by filtration

출처 및 근거

ORD 기록
ord-f0c86e4bd77944dfb5b53e3dff19e272
출처 데이터셋
uspto-grants-1982_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04347369

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트