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

Methylamine → Benzenemethanamine, N-methyl-3-(trifluoromethyl)-

HRID 711327
ノート
印刷プレビュー

反応式

HRID 711327 の反応式
[CH3:1][NH2:2].[F:3][C:4]([F:14])([F:13])[C:5]1[CH:6]=[C:7]([CH:10]=[CH:11][CH:12]=1)[CH2:8]Cl>CO>[CH3:1][NH:2][CH2:8][C:7]1[CH:10]=[CH:11][CH:12]=[C:5]([C:4]([F:14])([F:13])[F:3])[CH:6]=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

4

反応物 2

HCID 6329MethylamineHCID 697163-(Trifluoromethyl)benzyl chloride

生成物 1

HCID 485414Benzenemethanamine, N-methyl-3-(trifluoromethyl)-

試薬・触媒・溶媒 1

HCID 887Methanol溶媒3 回

反応条件

温度
50 °C

実験手順

To a solution of methylamine 2M in MeOH (61.5 mL, 123.3 mmol), MeOH (30 mL) was added. The mixture was heated at 50° C. under stirring and 3-(trifluoromethyl)benzyl chloride (1.6 mL, 10.3 mmol) dissolved in MeOH (10 mL) were added. The reaction mixture was stirred at this temperature for 5 h. The solvent was removed under vacuo, then NaOH 1M was added and the aqueous layer was extracted with DCM. The organic layer was filtered through a phase separator and concentrated in vacuo to give 2.19 g of a colourless oil. 1H NMR (400 MHz, CDCl3) δ ppm 7.69 (s, 1H), 7.57 (d, 1H), 7.49 (t, 2H), 3.88 (s, 2H), 2.56, (s, 3H). UPLC-MS: Rt=0.39; m/z (ES+): 190 [M+H]+.

後処理

  1. additionwere added
  2. stirringThe reaction mixture was stirred at this temperature for 5 h
  3. customThe solvent was removed under vacuo
  4. additionNaOH 1M was added
  5. extractionthe aqueous layer was extracted with DCM
  6. filtrationThe organic layer was filtered through a phase separator
  7. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-2568bcab23064cf68da054d7159941f9
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09181259B2

反応ノート

読み込み中…

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