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Glycine → N-(2-hydroxybenzyl)glycine

HRID 1267256
ノート
印刷プレビュー

反応式

HRID 1267256 の反応式
[NH2:1][CH2:2][C:3]([OH:5])=[O:4].[CH:6](=O)[C:7]1[C:8](=[CH:10][CH:11]=[CH:12][CH:13]=1)[OH:9].B.[Na]>[OH-].[Na+]>[OH:9][C:8]1[CH:10]=[CH:11][CH:12]=[CH:13][C:7]=1[CH2:6][NH:1][CH2:2][C:3]([OH:5])=[O:4]
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 3

HCID 750GlycineHCID 6998Salicylaldehyde2 回HCID 178418435HCID 178418435、化合物2 回

生成物 1

HCID 10726079N-(2-hydroxybenzyl)glycine

試薬・触媒・溶媒 1

HCID 14798Sodium Hydroxide溶媒

実験手順

Nine grams of glycine were dissolved in 60 ml of a 2N sodium hydroxide aqueous solution. To the solution were then added 12 ml of salicylaldehyde and 1.3 g of sodium boron hydride in this order. After the mixture was stirred for 1 hour, 12 ml of salicylaldehyde and 1.3 g of sodium boron hydride were added thereto again. After the resulting mixture was stirred at room temperature for 1 hour, the insoluble matter was separated through filtration, and the filtrate was extracted with diethyl ether. The extract was adjusted to a pH of 4 with hydrochloric acid to obtain 17 g of N-(2 -hydroxybenzyl) glycine. Various N-(2-hydroxybenzyl) amino acids were obtained in the same manner.

後処理

  1. stirringAfter the resulting mixture was stirred at room temperature for 1 hour
  2. customthe insoluble matter was separated through filtration
  3. extractionthe filtrate was extracted with diethyl ether

出典と根拠

ORDレコード
ord-0406807f8bd64375950f750f299593e4
出典データセット
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06552061B1

反応ノート

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