ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Phosphorus oxychloride → HCID 59362936、化合物

HRID 1668808
ノート
印刷プレビュー

反応式

HRID 1668808 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 24813Phosphorus oxychlorideHCID 178517420HCID 178517420、化合物

生成物 1

HCID 59362936HCID 59362936、化合物収率 86%

実験手順

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)

後処理

  1. temperaturewas heated
  2. temperatureto reflux for 4 hours
  3. customThereafter, volatiles were evaporated under reduced pressure
addition
the 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
  • 出典と根拠

    ORDレコード
    ord-43120d9f15e241e4b8d973c40b3626e9
    出典データセット
    uspto-grants-2011_08
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US07989463B2

    反応ノート

    読み込み中…

    このページの内容参加物実験手順後処理出典と根拠反応ノート