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Sulfuric Acid → 5-Hydroxy-1,2-dihydrophthalazin-1-one

HRID 838974
ノート
印刷プレビュー

反応式

HRID 838974 の反応式
S(=O)(=O)(O)O.N[C:7]1[CH:16]=[CH:15][CH:14]=[C:13]2[C:8]=1[CH:9]=[N:10][NH:11][C:12]2=[O:17].N([O-])=[O:19].[Na+].B(O)(O)O>O>[OH:19][C:7]1[CH:16]=[CH:15][CH:14]=[C:13]2[C:8]=1[CH:9]=[N:10][NH:11][C:12]2=[O:17]
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 4

HCID 1118Sulfuric Acid2 回HCID 7628Boric AcidHCID 123410025-amino-1(2H)-phthalazinoneHCID 23668193Sodium Nitrite

生成物 1

HCID 1357291005-Hydroxy-1,2-dihydrophthalazin-1-one収率 97%

試薬・触媒・溶媒 1

HCID 962Water溶媒3 回

実験手順

Concentrated sulphuric acid (8 ml) was added to a stirred mixture of 5-amino-1(2H)-phthalazinone (9.4 g, 0.058 mole) and water (50 ml). The resultant stirred paste was cooled in ice and diazotised by the addition of sodium nitrite (4.15 g, 0.06 mole) in water (15 ml). The filtered diazonium sulphate solution was added over 1.5 hours to a stirred boiling solution of concentrated sulphuric acid (30 ml) and boric acid (5.42 g, 0.088 mole) in water (200 ml). The solution was heated for a further 30 minutes then cooled and the collected solid was washed with water to give 5-hydroxy-1(2H)-phthalazinone 9.12 g, 96% m.p. 351°-355°). 5-Hydroxy-1(2H)-phthalazinone was purified as the 5-acetoxy derivative m.p. 162° (ethanol).

後処理

  1. temperaturewas cooled in ice
  2. temperatureThe solution was heated for a further 30 minutes
  3. temperaturethen cooled
  4. washthe collected solid was washed with water

出典と根拠

ORDレコード
ord-aa03621d27574beeb95979473212119c
出典データセット
uspto-grants-1978_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04093725

反応ノート

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