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Hydrochloric Acid → Methyl 2-(4-(aminomethyl)phenyl)acetate hydrochloride

HRID 1953003
ノート
印刷プレビュー

反応式

HRID 1953003 の反応式
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][C:10]([O:12][CH3:13])=[O:11])=[CH:5][CH:4]=1)#[N:2].[ClH:14].[H][H]>CO.[Pd]>[ClH:14].[CH3:13][O:12][C:10]([CH2:9][C:6]1[CH:7]=[CH:8][C:3]([CH2:1][NH2:2])=[CH:4][CH:5]=1)=[O:11]
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 3

HCID 313Hydrochloric AcidHCID 1512619Methyl (4-cyanophenyl)acetateHCID 178418361HCID 178418361、化合物

生成物 1

HCID 23301759Methyl 2-(4-(aminomethyl)phenyl)acetate hydrochloride

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

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

A solution of 8.8 g (0.05 Mol) of methyl 4-cyanobenzene acetate in 200 ml of methanol was hydrogenated, after the addition of 50 ml of 1 N aqueous hydrochloric acid and 3 g of palladium on activated charcoal (10%), at ambient temperature under a hydrogen pressure of 3 bar until the uptake of hydrogen had ended. The solution freed from catalyst was evaporated down, the residue was combined with two batches of 50 ml of toluene and evaporated down again. 10.7 g (99% of theory) of a crude crystalline material was obtained which was used without further purification in the next step.

後処理

  1. customat ambient temperature
  2. customwas evaporated down
  3. customevaporated down again
  4. custom10.7 g (99% of theory) of a crude crystalline material was obtained which
  5. customwas used without further purification in the next step

出典と根拠

ORDレコード
ord-8a064d04e48d430ab8b19ebb84afae13
出典データセット
uspto-grants-2000_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06114390

反応ノート

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