3-hydroxy-4-nitro-3H-isobenzofuran-1-one → 4-Amino-3-hydroxyphthalide

HRID 326809ノート

反応式

HRID 326809 の反応式
[OH:1][CH:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][C:10]=2[N+:12]([O-])=O)[C:4](=[O:5])[O:3]1>O1CCCC1.[Pd]>[NH2:12][C:10]1[CH:9]=[CH:8][CH:7]=[C:6]2[C:11]=1[CH:2]([OH:1])[O:3][C:4]2=[O:5]

参加物

4

反応物 1

HCID 110955283-hydroxy-4-nitro-3H-isobenzofuran-1-one

生成物 1

HCID 151807284-Amino-3-hydroxyphthalide

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 8028Tetrahydrofuran溶媒

実験手順

10 g of 3-hydroxy-4-nitro-phthalide are dissolved in 100 ml of tetrahydrofuran and, after addition of 1 g of palladium on barium sulphate (5%), the mixture is hydrogenated at atmospheric pressure and 20°-25° C. The catalyst is filtered off and the filtrate is concentrated. The evaporation residue is stirred with ether and filtered off with suction. 5.8 g (68.5% of theory) of a colourless substance of melting point 280°-285° C. (dec.) are obtained.

後処理

  1. customis hydrogenated at atmospheric pressure and 20°-25° C
  2. filtrationThe catalyst is filtered off
  3. concentrationthe filtrate is concentrated
  4. filtrationfiltered off with suction
  5. custom5.8 g (68.5% of theory) of a colourless substance of melting point 280°-285° C. (dec.) are obtained

出典と根拠

ORDレコード
ord-cf5750770f3449e0a1550b7a704f6820
出典データセット
uspto-grants-1993_12
特許番号
US05270469

反応ノート

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