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

Hydrochloric Acid → 2-(2-Aminophenyl)propan-2-ol

HRID 1377690
ノート
印刷プレビュー

反応式

HRID 1377690 の反応式
C[Mg]Br.[NH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[C:11](=[O:13])[CH3:12].Cl.[C:15](=O)(O)[O-].[Na+]>C1(C)C=CC=CC=1.C1COCC1>[NH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[C:11]([CH3:15])([CH3:12])[OH:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 110862'-AminoacetophenoneHCID 516892Sodium BicarbonateHCID 178418573HCID 178418573、化合物

生成物 1

HCID 2535272-(2-Aminophenyl)propan-2-ol

試薬・触媒・溶媒 2

HCID 1140Toluene溶媒HCID 8028
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
Tetrahydrofuran
溶媒

実験手順

To a 0° C. solution of methylmagnesium bromide (45 mL of a 1.4M solution in toluene, 63 mmol) under nitrogen atmosphere was added a solution of ortho-aminoacetophenone (2.9 g, 21.5 mmol) in THF (20 mL). The mixture was warmed to ambient temperature for 45 min, cooled to 0° C., and poured into ice-water. The mixture was acidified with 6N HCl, adjusted to ca. pH 6 with saturated sodium bicarbonate solution, and then extracted with ether (2×100 mL). The combined ether fractions were dried (MgSO4), filtered and the solvent was removed under reduced pressure to give the oily product, 2-aminophenyldimethyl carbinol.

後処理

  1. temperaturecooled to 0° C.
  2. extractionextracted with ether (2×100 mL)
  3. dry with materialThe combined ether fractions were dried (MgSO4)
  4. filtrationfiltered
  5. customthe solvent was removed under reduced pressure

出典と根拠

ORDレコード
ord-d131bc12c93947f99fe94a35ae46405c
出典データセット
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05665719

反応ノート

読み込み中…