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

Phosphorus oxychloride → HCID 59362936, 화합물

HRID 1668808
노트
인쇄 미리보기

반응식

HRID 1668808 반응식
[CH:1]1([C:6]2[N:11]=[C:10](O)[C:9]3[CH2:13][CH2:14][CH2:15][C:8]=3[N:7]=2)[CH2:5][CH2:4][CH2:3][CH2:2]1.P(Cl)(Cl)([Cl:18])=O>>[Cl:18][C:10]1[C:9]2[CH2:13][CH2:14][CH2:15][C:8]=2[N:7]=[C:6]([CH:1]2[CH2:5][CH2:4][CH2:3][CH2:2]2)[N:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 178517420HCID 178517420, 화합물

생성물 1

HCID 59362936HCID 59362936, 화합물수율 86%

실험 절차

A mixture of 2-cyclopentyl-6,7-dihydro-5H-cyclopentapyrimidin-4-ol (4.5 g, 22 mmol) and phosphorus oxychloride (13 mL, 130 mmol) was heated to reflux for 4 hours. Thereafter, volatiles were evaporated under reduced pressure and the mixture was poured over ice-water. After stirring for 1 hour, the product was extracted with dichloromethane (3×50 mL). The combined organic extracts were washed with water, treated with activated charcoal, dried over anhydrous Na2SO4, filtered, and the filtrate was concentrated under reduced pressure to afford the title compound as a light yellow solid (4.2 g, 86% yield)

후처리

  1. temperaturewas heated
  2. temperatureto reflux for 4 hours
  3. customThereafter, volatiles were evaporated under reduced pressure
  • additionthe mixture was poured over ice-water
  • extractionthe product was extracted with dichloromethane (3×50 mL)
  • washThe combined organic extracts were washed with water
  • additiontreated with activated charcoal
  • dry with materialdried over anhydrous Na2SO4
  • filtrationfiltered
  • concentrationthe filtrate was concentrated under reduced pressure
  • 출처 및 근거

    ORD 기록
    ord-43120d9f15e241e4b8d973c40b3626e9
    출처 데이터셋
    uspto-grants-2011_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07989463B2

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트