Iodine → 7-Bromo-5-cyanomethyl-2-nitro-3-phenylbenzofuran

HRID 262093

反応式

HRID 262093 の反応式
[C:1]([CH2:3][C:4]1[CH:5]=[C:6]([Br:20])[C:7]2[O:11][C:10](Br)=[C:9]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[C:8]=2[CH:19]=1)#[N:2].[N+:21]([O-:26])([N+]([O-])=O)=[O:22].C1CCC(C(O)=O)CC=1.II.S([O-])([O-])(=O)=S.[Na+].[Na+]>C(Cl)(Cl)Cl>[Br:20][C:6]1[C:7]2[O:11][C:10]([N+:21]([O-:26])=[O:22])=[C:9]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[C:8]=2[CH:19]=[C:4]([CH2:3][C:1]#[N:2])[CH:5]=1

参加物

7

反応物 5

HCID 807IodineHCID 209033-Cyclohexene-1-carboxylic acid2 回HCID 24477Sodium ThiosulfateHCID 25352Nitrogen oxide (N2O4)2 回HCID 213199065-Cyanomethyl-2,7-dibromo-3-phenylbenzofuran

生成物 1

HCID 213199467-Bromo-5-cyanomethyl-2-nitro-3-phenylbenzofuran

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

A solution containing 11.1 g. (0.028 mole) of 5-cyanomethyl-2,7-dibromo-3-phenylbenzofuran, 10.7 g. (0.11 mole) of dinitrogen tetroxide, 13.9 g. (0.11 mole) of cyclohexene-4-carboxylic acid and 1 g. of iodine in 500 ml. of chloroform is stirred at room temperature for 16 hours. An additional 13.9 g. of cyclohexene-4-carboxylic acid and 10.7 g. of dinitrogen tetroxide are added, and stirring is continued for 16 hours. The reaction is then treated with 500 ml. of 10 percent sodium thiosulfate. The phases are separated, and the organic phase is washed thrice with 250 ml. portions of saturated sodium bicarbonate, once with 250 ml. of 3 N hydrochloric acid and dried. Evaporation gives 7-bromo-5-cyanomethyl-2-nitro-3-phenylbenzofuran as a yellow solid, recrystallized from ethyl acetate-hexane to give a sample for analysis.

後処理

  1. additionA solution containing 11.1 g
  2. additionThe reaction is then treated with 500 ml
  3. customThe phases are separated
  4. washthe organic phase is washed thrice with 250 ml
  5. dry with materialof 3 N hydrochloric acid and dried
  6. customEvaporation

出典と根拠

ORDレコード
ord-fb0bd4904a8842a48622e57779dcca46
出典データセット
uspto-grants-1979_05
特許番号
US04153619

関連ノート

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