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

Acetyl chloride → (R)-1-methoxy-4,4-dimethyl-1-oxopentan-3-aminium chloride

HRID 2171831
ノート
印刷プレビュー

反応式

HRID 2171831 の反応式
[NH2:1][C@@H:2]([C:7]([CH3:10])([CH3:9])[CH3:8])[CH2:3][C:4]([OH:6])=[O:5].[C:11]([Cl:14])(=O)C>CO>[Cl-:14].[CH3:11][O:5][C:4](=[O:6])[CH2:3][C@@H:2]([NH3+:1])[C:7]([CH3:10])([CH3:9])[CH3:8]
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

4

反応物 2

HCID 6367Acetyl chlorideHCID 7010080(R)-3-Amino-4,4-dimethylpentanoic acid

生成物 1

HCID 86714730(R)-1-methoxy-4,4-dimethyl-1-oxopentan-3-aminium chloride

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
65 °C

実験手順

(R)-3-amino-4,4-dimethylpentanoic acid, 2a, was dissolved in methanol (1.4 L). The solution was cooled in an ice bath and acetyl chloride (67.0 mL, 947.0 mmol) was added dropwise (maintaining the temperature below 10° C.). The reaction mixture was heated to 65° C. and stirred at that temperature for 3 h. The reaction mixture was cooled to room temperature and then flushed with toluene to remove volatiles. The crude material was used without further purification: 1H NMR (400 MHz, MeOH-d4) δ 3.75 (s, 3H), 3.41 (t, 1H), 2.88 (dd, 1H), 2.64-2.46 (m, 1H), 1.04 (s, 9H).

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

後処理

  1. temperatureThe solution was cooled in an ice bath
  2. temperaturemaintaining the temperature below 10° C.)
  3. temperatureThe reaction mixture was cooled to room temperature
  4. customflushed with toluene
  5. customto remove volatiles
  6. customThe crude material was used without further purification

出典と根拠

ORDレコード
ord-09e48850336e4b189079ccb823904d0f
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09051319B2

反応ノート

読み込み中…