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

Ammonia → 4-Cyclopropyl-6-(trichloromethyl)-1,3,5-triazin-2-amine

HRID 462337
노트
인쇄 미리보기

반응식

HRID 462337 반응식
[CH:1]1([C:4]2[N:9]=[C:8]([C:10]([Cl:13])([Cl:12])[Cl:11])[N:7]=[C:6](C(Cl)(Cl)Cl)[N:5]=2)[CH2:3][CH2:2]1.[NH3:18]>O1CCCC1.O>[NH2:18][C:6]1[N:5]=[C:4]([CH:1]2[CH2:2][CH2:3]2)[N:9]=[C:8]([C:10]([Cl:13])([Cl:12])[Cl:11])[N:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 222AmmoniaHCID 201996132-Cyclopropyl-4,6-bis-trichloromethyl-1,3,5-triazine

생성물 1

HCID 201996154-Cyclopropyl-6-(trichloromethyl)-1,3,5-triazin-2-amine

시약·촉매·용매 2

HCID 962Water용매HCID 8028Tetrahydrofuran용매

실험 절차

71.2 g of 2-cyclopropyl-4,6-bis-trichloromethyl-1,3,5-triazine are dissolved in 70 ml of tetrahydrofuran, and at room temperature are added, with stirring, 300 ml of a concentrated aqueous ammonia solution. The reaction mixture is stirred for 30 minutes; it is then diluted with water, and the formed emulsion is extracted with ether. The ether phases are collected, dried, filtered and subsequently concentrated by evaporation. The residue crystallises and there remain 48 g of the crystalline title product, m.p. 111°-114° C.

후처리

  1. additionat room temperature are added
  2. stirringThe reaction mixture is stirred for 30 minutes
  3. extractionthe formed emulsion is extracted with ether
  4. customThe ether phases are collected
  5. customdried
  6. filtrationfiltered
  7. concentrationsubsequently concentrated by evaporation
  8. customThe residue crystallises

출처 및 근거

ORD 기록
ord-ba860c4d9f1944969d96c928f25b2391
출처 데이터셋
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04515626

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트