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

3-Chloropropionyl chloride → HCID 21074075, 화합물

HRID 1373059
노트
인쇄 미리보기

반응식

HRID 1373059 반응식
[NH2:1][C:2]1[CH:15]=[CH:14][C:13]2[NH:12][C:11]3[C:6](=[CH:7][C:8]([NH2:16])=[CH:9][CH:10]=3)[C:5](=[O:17])[C:4]=2[CH:3]=1.[Cl:18][CH2:19][CH2:20][C:21](Cl)=[O:22]>>[Cl:18][CH2:19][CH2:20][C:21]([NH:16][C:8]1[CH:9]=[CH:10][C:11]2[NH:12][C:13]3[C:4](=[CH:3][C:2]([NH:1][C:21](=[O:22])[CH2:20][CH2:19][Cl:18])=[CH:15][CH:14]=3)[C:5](=[O:17])[C:6]=2[CH:7]=1)=[O:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 693643-Chloropropionyl chlorideHCID 210740792,7-Diaminoacridin-9(10H)-one

생성물 1

HCID 21074075HCID 21074075, 화합물수율 81%

실험 절차

A suspension of 2,7-diamino-9(10H)-acridone 12 (13.44 g, 60 mmol), in 3-chloropropionyl chloride (3-CPC) (240 mL) was stirred at 90° C. for 4 hr and then heated under reflux for 2 hr. The resultant mixture was cooled to 0° C. after which the product was collected on a glass sinter. The product was washed with acetone (60 mL) followed by toluene (2×60 mL), more acetone (4×60 mL), dry ether (2×60 mL) and finally hexane (2×60 mL). The product was dried over P2O5 under vacuum to yield an olive-green solid (19.68 g, 81%).

후처리

  1. temperatureheated
  2. temperatureunder reflux for 2 hr
  3. customwas collected on a glass sinter
  4. washThe product was washed with acetone (60 mL)
  • dry with materialThe product was dried over P2O5 under vacuum
  • 출처 및 근거

    ORD 기록
    ord-742a9fbd175a4eb6a750f97d57405e40
    출처 데이터셋
    uspto-grants-2007_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07160896B2

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트