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

Phosgene → HCID 21072848、化合物

HRID 1372900
ノート
印刷プレビュー

反応式

HRID 1372900 の反応式
[C:1](Cl)(Cl)=[O:2].[NH2:5][C:6]1[CH:11]=CC=C[C:7]=1C(O)(C)C.N[CH2:17][C:18](C1C=CC=CC=1)=O.C[Mg]I.[CH2:29]1[CH2:33][O:32][CH2:31][CH2:30]1>>[CH3:7][C:6]1([CH3:11])[C:30]2[CH:29]=[CH:33][CH:17]=[CH:18][C:31]=2[O:32][C:1](=[O:2])[NH:5]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 5

HCID 6371PhosgeneHCID 8028Tetrahydrofuran2 回HCID 11952PhenacylamineHCID 2535272-(2-Aminophenyl)propan-2-olHCID 178418373HCID 178418373、化合物

生成物 1

HCID 21072848HCID 21072848、化合物

実験手順

112 g (1.13 mol) phosgene are piped into 500 mL THF. Then a solution of 52 g (0.34 mol) 2-(2-amino-phenyl)-propan-2-ol, prepared from 2-aminoacetophenone and methylmagnesium iodide, in 300 mL THF is added. The reaction mixture is left to stand overnight, evaporated down and combined with 500 ml pyridine. After the pyridine has been distilled off water is added and the mixture is extracted with diethyl ether. The organic phases are washed successively with 2 N hydrochloric acid, sodium hydroxide solution and water, dried with sodium sulphate and evaporated down. The residue remaining (46 g) is further reacted directly without any more purification.

後処理

  1. additionis added
  2. waitThe reaction mixture is left
  3. customevaporated down
  4. distillationAfter the pyridine has been distilled off water
  5. additionis added
  6. extractionthe mixture is extracted with diethyl ether
  7. washThe organic phases are washed successively with 2 N hydrochloric acid, sodium hydroxide solution and water
  8. dry with materialdried with sodium sulphate
  9. customevaporated down
  10. customis further reacted directly without any more purification

出典と根拠

ORDレコード
ord-dae4c0f8100449db99fdd854c66b7f30
出典データセット
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07160882B2

反応ノート

読み込み中…

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