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Diazomethane → 2-Isopropoxyimino-2-phenylacetic acid

HRID 328456
ノート
印刷プレビュー

反応式

HRID 328456 の反応式
[C:1]1([C:7](=O)[C:8]([OH:10])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl.[CH:13]([O:16][NH2:17])([CH3:15])[CH3:14].[OH-].[Na+].[N+](=C)=[N-]>O.C(O)C>[CH:13]([O:16][N:17]=[C:7]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)[C:8]([OH:10])=[O:9])([CH3:15])[CH3:14]
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 9550DiazomethaneHCID 11915Phenylglyoxylic AcidHCID 14798Sodium Hydroxide2 回HCID 12696235O-(propan-2-yl)hydroxylamine hydrochloride

生成物 1

HCID 542830792-Isopropoxyimino-2-phenylacetic acid収率 97.6%

試薬・触媒・溶媒 2

HCID 702Ethanol
溶媒
HCID 962Water溶媒

実験手順

A mixture of phenylglyoxylic acid (3.0 g.), isopropoxyamine hydrochloride (2.5 g.), ethanol (100 ml) and water (50 ml) was stirred and adjusted to pH 4.5 to 5 with sodium hydroxide solution (2N). The solution was stirred for 5 hr. maintaining the pH at 4.5-5 with further additions of sodium hydroxide solution. The ethanol was removed by evaporation, the aqueous residue acidified and the product collected by extraction with ethyl acetate. Evaporation of the ethyl acetate gave a brown oil (4.2 g.). that was esterified conventionally with diazomethane to give a mixture of the syn and anti methyl esters of the title compound as an oil (4.04 g.).

後処理

  1. stirringThe solution was stirred for 5 hr
  2. customThe ethanol was removed by evaporation
  3. customthe product collected by extraction with ethyl acetate
  4. customEvaporation of the ethyl acetate
  5. customgave a brown oil (4.2 g.)
  6. customto give

出典と根拠

ORDレコード
ord-a629001ca31647a0bd465725c63cd119
出典データセット
uspto-grants-1977_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04017515

反応ノート

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