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Acetic Acid → 4,5,6-Triethoxy-7-nitrophthalide

HRID 1788794
ノート
印刷プレビュー

反応式

HRID 1788794 の反応式
C(O)(=O)C.[CH2:5]([O:7][C:8]1[C:17]([O:18][CH2:19][CH3:20])=[C:16]([O:21][CH2:22][CH3:23])[CH:15]=[C:14]2[C:9]=1[CH2:10][O:11][C:12]2=[O:13])[CH3:6].[N+:24]([O-])([OH:26])=[O:25]>O>[CH2:5]([O:7][C:8]1[C:17]([O:18][CH2:19][CH3:20])=[C:16]([O:21][CH2:22][CH3:23])[C:15]([N+:24]([O-:26])=[O:25])=[C:14]2[C:9]=1[CH2:10][O:11][C:12]2=[O:13])[CH3:6]
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 176Acetic AcidHCID 944Nitric AcidHCID 133178834,5,6-Triethoxyphthalide

生成物 1

HCID 64521774,5,6-Triethoxy-7-nitrophthalide収率 35%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Glacial acetic acid (14 ml) was added to 5.32 g (0.02 mole) of 4,5,6-triethoxyphthalide. Into the reaction mixture on a water bath at 30-35° C., 14 ml of fuming nitric acid, d=1.52, was gradually added dropwise over a time period of 9 hours. After completion of the addition, the reaction mixture was allowed to stand overnight at room temperature and thereafter 80 ml of water was added to deposit crystals. The crystals were filtered out, washed thoroughly with water and dried. There was obtained 2.20 g of 4,5,6-triethoxy-7-nitrophthalide having a melting point of 82.5-84.5° C. with a yield of 35%.

後処理

  1. additionAfter completion of the addition
  2. filtrationThe crystals were filtered out
  3. washwashed thoroughly with water
  4. customdried

出典と根拠

ORDレコード
ord-2a9efe2e38d441bdb33e0120ea48ea1f
出典データセット
uspto-grants-1987_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04684732

反応ノート

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