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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
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Water → HCID 22253670、化合物

HRID 1064547
ノート
印刷プレビュー

反応式

HRID 1064547 の反応式
[NH2:1][C:2]([CH3:7])([CH3:6])[C:3]([OH:5])=[O:4].[OH-].[Na+].O.[Br:11][CH:12]([CH3:16])[C:13](Br)=[O:14]>C(Cl)(Cl)Cl>[Br:11][CH:12]([CH3:16])[C:13]([NH:1][C:2]([CH3:7])([CH3:6])[C:3]([OH:5])=[O:4])=[O:14]
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 4

HCID 962WaterHCID 6119Aminoisobutyric acidHCID 14798Sodium HydroxideHCID 79047Propanoyl bromide, 2-bromo-

生成物 1

HCID 22253670HCID 22253670、化合物

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒2 回

反応条件

温度
このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート
-12 °C

実験手順

To a stirring mixture of 2-aminoisobutyric acid (52.08 g, 0.51 mol), sodium hydroxide (20.20 g, 0.51 mol), 200 mL water, and 50 mL chloroform cooled to −12° C., was added a solution of 2-bromopropionyl bromide (100 g, 0.46 mol) in 150 mL chloroform over 15 minutes. The temperature was maintained between −15 and −12° C. during the addition. The reaction mixture was then allowed to warm to room temperature and the precipitated solid was filtered. The solid was mixed with 700 mL hot toluene, and then cooled. The white solid was then filtered and dried under vacuum. A yield of 77.60 g (70%) was obtained.

後処理

  1. temperatureThe temperature was maintained between −15 and −12° C. during the addition
  2. temperatureto warm to room temperature
  3. filtrationthe precipitated solid was filtered
  4. additionThe solid was mixed with 700 mL hot toluene
  5. temperaturecooled
  6. filtrationThe white solid was then filtered
  7. customdried under vacuum
  8. customA yield of 77.60 g (70%) was obtained

出典と根拠

ORDレコード
ord-65929cf8ae0640f0aaa83641c2cb9974
出典データセット
uspto-grants-2005_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06969749B2

反応ノート

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