Acetic Acid → 1,2,3,4,9,9-Hexachloro-1,4,4a,6,7,8a-hexahydro-1,4-methanonaphthalene-5,8-dione

HRID 436590

反応式

HRID 436590 の反応式
[Cl:1][C:2]12[C:14]([Cl:16])([Cl:15])[C:5]([Cl:17])([CH:6]3[CH:11]1[C:10](=[O:12])[CH:9]=[CH:8][C:7]3=[O:13])[C:4]([Cl:18])=[C:3]2[Cl:19].C(O)(=O)C.O>[Zn].C(Cl)(Cl)Cl>[Cl:1][C:2]12[C:14]([Cl:15])([Cl:16])[C:5]([Cl:17])([CH:6]3[CH:11]1[C:10](=[O:12])[CH2:9][CH2:8][C:7]3=[O:13])[C:4]([Cl:18])=[C:3]2[Cl:19]

参加物

6

反応条件

温度
50 °C

実験手順

38 g. of 1,2,3,4,9,9-hexachloro-1,4,4a,8a-tetrahydro-1,4-methanonaphthalene-5,8-dione, prepared as in Example 1, were suspended in 150 ml. of glacial acetic acid and then this mixture was poured into 20 g. of zinc dust suspended in 150 ml. of distilled water. A slight exotherm occurred during stirring and the temperature was maintained at 50° C. for 3 hours by external heating. Then 200 ml. of chloroform were added and stirring was continued for 30 minutes more. The chloroform layer was separated and washed with a saturated sodium carbonate solution and dried over anhydrous magnesium sulfate. Evaporation of the chloroform left a white solid. One recrystallization from methanol gave white crystals, m.p. 169°-170° C. Infrared spectrum showed carbonyl at 1740 cm-1. The nmr indicated two bridgehead protons at 431 Hz (singlet) and four α- protons at 303 Hz and 245 Hz (as a multiplet).

後処理

  1. stirringstirring
  2. customThe chloroform layer was separated
  3. washwashed with a saturated sodium carbonate solution
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customEvaporation of the chloroform
  6. waitleft a white solid
  7. customOne recrystallization from methanol
  8. customgave white crystals, m.p. 169°-170° C

出典と根拠

ORDレコード
ord-692d4b709d32420da0df7d9a5c8a9fd8
出典データセット
uspto-grants-1977_02
特許番号
US04009200

関連ノート

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