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Hydrochloric Acid → 3-(Aminomethyl)phenol hydrochloride

HRID 1058372
ノート
印刷プレビュー

反応式

HRID 1058372 の反応式
[C:1]([C:3]1[CH:4]=[C:5]([OH:9])[CH:6]=[CH:7][CH:8]=1)#[N:2].[ClH:10]>C(O)C.[Pd]>[ClH:10].[OH:9][C:5]1[CH:4]=[C:3]([CH:8]=[CH:7][CH:6]=1)[CH2:1][NH2:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 313Hydrochloric AcidHCID 133943-Cyanophenol

生成物 1

HCID 220584273-(Aminomethyl)phenol hydrochloride収率 71.8%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

To a solution of 3-cyanophenol (30 g, 0.252 mol) in ethanol (150 mL) at 25° C. under an atmosphere of nitrogen, was added 10% palladium on carbon (3 g) ) followed by concentrated hydrochloric acid solution (23 mL, 0.277 mol). The reaction mixture was hydrogenated at 50 psi in a Parr apparatus for 2.5 h and was then filtered over Celite® and washed well with ethanol (100 mL). The solvents were concentrated under reduced pressure and the resulting solid was placed under vacuum for 1 h. The solid was dissolved in 150 mL of hot ethanol, filtered and crystallized by adding diethyl ether. The solids were collected by filtration, washed well with diethyl ether and dried under vacuum 24 h to give 3-hydroxybenzylamine hydrochloride (28.88 g, 71% yield) as a colorless solid.

後処理

  1. filtrationwas then filtered over Celite®
  2. washwashed well with ethanol (100 mL)
  3. concentrationThe solvents were concentrated under reduced pressure
  4. waitthe resulting solid was placed under vacuum for 1 h
  5. dissolutionThe solid was dissolved in 150 mL of hot ethanol
  6. filtrationfiltered
  7. customcrystallized
  8. additionby adding diethyl ether
  9. filtrationThe solids were collected by filtration
  10. washwashed well with diethyl ether
  11. customdried under vacuum 24 h

出典と根拠

ORDレコード
ord-4e965a2cb2654868857a0a4434e7c2ad
出典データセット
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06515124B2

反応ノート

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