Sodium Hydroxide → 2,5-Diaminoanisole

HRID 1732862

反応式

HRID 1732862 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([NH2:9])[CH:6]=[CH:5][C:4]=1[NH2:10].OS(O)(=O)=O.[OH-].[Na+]>O>[CH3:1][O:2][C:3]1[CH:8]=[C:7]([NH2:9])[CH:6]=[CH:5][C:4]=1[NH2:10]

参加物

4

反応物 2

HCID 14798Sodium HydroxideHCID 923741,4-Benzenediamine, 2-methoxy-, sulfate

生成物 1

HCID 213792,5-Diaminoanisole収率 79.6%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

2-Methoxy-p-phenylenediamine-H2SO4 (100 g) is stirred for an hour in a solution containing 42 g of NaOH in 550 ml of H2O. The diamine is extracted eleven times successively with 200 ml of CH2Cl2 and the combined extracts are dried over MgSO4. The extract is filtered and evaporated to dryness in vacuo to afford 43 g (79.6% recovery) of 2-methoxy-p-phenylenediamine. The solid diamine then is added to diethoxyphosphinyl isothiocyanate (or diethyl phosphoroisothiocyanatidate prepared by stirring 134.4 g of diethyl phosphorchloridate with 66 g of dry NaSCN in 150 ml of CH2Cl2) in CH2Cl2. An additional 300 ml of CH2Cl2 is added and after 23 hours at ambient temperature, the mixture is warmed to reflux temperature on a steam bath. The mixture is cooled and 400 ml of water is added and after shaking, the organic phase is separated. The organic phase is treated with charcoal and evaporated to dryness to afford a brown residue. This residue is stirred in 100 ml of acetone/240 ml of pentane and filtered to give 118 g (72%) of the title compound. The overall yield including the isolation of the diamine is 57.6%.

後処理

  1. extractionThe diamine is extracted eleven times successively with 200 ml of CH2Cl2
  2. dry with materialthe combined extracts are dried over MgSO4
  3. filtrationThe extract is filtered
  4. customevaporated to dryness in vacuo

出典と根拠

ORDレコード
ord-cf52ab1cbc7b4ee988b6cc83eb211dc2
出典データセット
uspto-grants-1980_12
特許番号
US04239708

関連ノート

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