Hydrochloric Acid → Benzoic acid, 3,4-dihydroxy-5-nitro-, methyl ester
反応式
[OH:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([N+:12]([O-:14])=[O:13])[C:10]=1[OH:11])[C:5]([OH:7])=[O:6].Cl.[CH2:16](Cl)Cl>>[OH:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([N+:12]([O-:14])=[O:13])[C:10]=1[OH:11])[C:5]([O:7][CH3:16])=[O:6]参加物
4
実験手順
1.0 g of 3,4-dihydroxy-5-nitrobenzoic acid is treated with 20 ml of methanolic hydrochloric acid, stirred at 45° for 3 hours and, after removing the solvent, the residue is taken up in methylene chloride. The organic phase is washed with sodium chloride solution, dried over sodium sulfate and evaporated. The crystalline product obtained is taken up in methylene chloride and filtered over a ten-fold amount of silica gel. The material obtained is recrystallized from ethyl acetate/n-hexane. There is obtained methyl 3,4-dihydroxy-5-nitrobenzoate in the form of yellow crystals of m.p. 144°-145°.
後処理
- customafter removing the solvent
- washThe organic phase is washed with sodium chloride solution
- dry with materialdried over sodium sulfate
- customevaporated
- customThe crystalline product obtained
- filtrationfiltered over a ten-fold amount of silica gel
- customThe material obtained
- customis recrystallized from ethyl acetate/n-hexane
出典と根拠
- ORDレコード
- ord-53fbf10e2c4441aea8e6b040c2287145
- 出典データセット
- uspto-grants-1998_01
- 特許番号
- US05705703
反応ノート
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