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

HCID 68552376、化合物 → 460078-00-6

HRID 1816850
ノート
印刷プレビュー

反応式

HRID 1816850 の反応式
COC1C=CC(C[NH:8][CH2:9][CH2:10][CH:11]([CH2:24][CH2:25][NH:26]CC2C=CC(OC)=CC=2)[CH2:12][CH2:13][NH:14]CC2C=CC(OC)=CC=2)=CC=1>CO.[OH-].[OH-].[Pd+2]>[NH2:8][CH2:9][CH2:10][CH:11]([CH2:24][CH2:25][NH2:26])[CH2:12][CH2:13][NH2:14]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 68552376HCID 68552376、化合物

生成物 1

HCID 9942175460078-00-6収率 50%

試薬・触媒・溶媒 2

HCID 9942167Palladium hydroxide触媒2 回HCID 887Methanol溶媒

実験手順

1,1,1-tris[2(p-methoxybenzylamino)ethyl]methane (20.0 gram, 0.036 mol) was dissolved in methanol (100 ml) and Pd(OH)2 (5.0 gram) was added. The mixture was hydrogenated (3 bar, 100° C., in an autoclave) and stirred for 5 hours. Pd(OH)2 was added in two more portions (2×5 gram) after 10 and 15 hours respectively. The reaction mixture was filtered and the filtrate was washed with methanol. The combined organic phase was evaporated and the residue was distilled under vacuum (1×10−2, 110° C.) to give 2.60 gram (50%) of 1,1,1-tris(2-aminoethyl)methane identical with the previously described Example 1.

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

後処理

  1. custom3 bar, 100° C.
  2. filtrationThe reaction mixture was filtered
  3. washthe filtrate was washed with methanol
  4. customThe combined organic phase was evaporated
  5. distillationthe residue was distilled under vacuum (1×10−2, 110° C.)

出典と根拠

ORDレコード
ord-5841f21f61df437987ab149fcc5db054
出典データセット
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07597875B2

反応ノート

読み込み中…