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N-(o-Nitrobenzyl)ethyl glycine → N-(o-Aminobenzyl)ethyl glycine

HRID 1263155
ノート
印刷プレビュー

反応式

HRID 1263155 の反応式
[N+:1]([C:4]1[CH:17]=[CH:16][CH:15]=[CH:14][C:5]=1[CH2:6][CH2:7][CH2:8][NH:9][CH2:10][C:11]([OH:13])=[O:12])([O-])=O.[H][H]>[Pd].C(O)C>[NH2:1][C:4]1[CH:17]=[CH:16][CH:15]=[CH:14][C:5]=1[CH2:6][CH2:7][CH2:8][NH:9][CH2:10][C:11]([OH:13])=[O:12]
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 57139570N-(o-Nitrobenzyl)ethyl glycineHCID 178418361HCID 178418361、化合物

生成物 1

HCID 57043355N-(o-Aminobenzyl)ethyl glycine収率 77%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

To a solution of 13.0 g. (5.46×10-2 moles) of N-(o-nitrobenzyl)ethyl glycine in 200 ml. of absolute ethyl alcohol was added slowly 0.76 g. (5% by weight) of 10% Pd/C catalyst and the mixture placed on a Paar hydrogenator. The mixture was shaken until theoretical hydrogen (16.4×10-2 moles) had been absorbed, removed from the Paar and the mixture filtered under suction. The catalyst was washed with ethyl alcohol and the solvent removed in vacuo affording a yellow oil. Purification of the oil was effected by distillation yielding 8.8 g. (77% yield) of a colorless oil; b.p. 124°-126° C. (0.03 mm).

後処理

  1. customhad been absorbed
  2. customremoved from the Paar
  3. filtrationthe mixture filtered under suction
  4. washThe catalyst was washed with ethyl alcohol
  5. customthe solvent removed in vacuo
  6. customaffording a yellow oil
  7. customPurification of the oil
  8. distillationwas effected by distillation
  9. customyielding 8.8 g

出典と根拠

ORDレコード
ord-72362217f34f4702a5aefb4584a3e203
出典データセット
uspto-grants-1984_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
USRE031617

反応ノート

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