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Cyanuric chloride → 3-(4,6-Dichloro-1,3,5-triazin-2-yl)-8-oxa-3-azabicyclo[3.2.1]octane

HRID 536837
ノート
印刷プレビュー

反応式

HRID 536837 の反応式
[N:1]1[C:8]([Cl:9])=[N:7][C:5](Cl)=[N:4][C:2]=1[Cl:3].Cl.[CH:11]12[O:18][CH:15]([CH2:16][CH2:17]1)[CH2:14][NH:13][CH2:12]2>CC(C)=O.O.C([O-])(O)=O.[Na+]>[Cl:9][C:8]1[N:1]=[C:2]([Cl:3])[N:4]=[C:5]([N:13]2[CH2:12][CH:11]3[O:18][CH:15]([CH2:16][CH2:17]3)[CH2:14]2)[N:7]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 2

HCID 7954Cyanuric chlorideHCID 219835368-Oxa-3-aza-bicyclo(3.2.1)octane hydrochloride

生成物 1

HCID 579682473-(4,6-Dichloro-1,3,5-triazin-2-yl)-8-oxa-3-azabicyclo[3.2.1]octane収率 60.8%

試薬・触媒・溶媒 3

HCID 180Acetone溶媒2 回HCID 962Water溶媒
HCID 516892
Sodium Bicarbonate
溶媒

反応条件

温度
0 °C

実験手順

To a solution of cyanuric chloride (2.00 g, 10.85 mmoles) in acetone (20 mL) and water (10 mL) at 0° C. was added a solution of 8-oxa-3-azabicyclo[3.2.1]octane hydrochloride (1.46 g, 9.76 mmoles) in saturated aqueous NaHCO3 (25 mL) and acetone (25 mL) via addition funnel over 15 minutes. The reaction was stirred at 0° C. for 2 hours, then filtered to collect a white precipitate. The precipitate was washed with water (25 mL) and dried. The crude product was purified by column chromatography (30:70 ethyl acetate in hexanes) to provide 3-(4,6-dichloro-1,3,5-triazin-2-yl)-8-oxa-3-azabicyclo[3.2.1]octane (1.55 g) as a white solid.

後処理

  1. additionvia addition funnel over 15 minutes
  2. filtrationfiltered
  3. customto collect a white precipitate
  4. washThe precipitate was washed with water (25 mL)
  5. customdried
  6. customThe crude product was purified by column chromatography (30:70 ethyl acetate in hexanes)

出典と根拠

ORDレコード
ord-970abcfe98584df19613528ac1726e7b
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08859542B2

反応ノート

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