Benzenesulfinic acid → 1,2,3,4,9,9-Hexachloro-1,4,4a,6,7,8a-hexahydro-6-phenylsulfonyl-1,4-methanonaphthalene-5,8-dione

HRID 46692

反応式

HRID 46692 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:20]1([S:26]([OH:28])=[O:27])[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>O.C1C=CC=CC=1>[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][CH:8]([S:26]([C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)(=[O:28])=[O:27])[C:7]3=[O:13])[C:4]([Cl:18])=[C:3]2[Cl:19]

参加物

5

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 dissolved in 250 ml. of benzene, 15 g. of freshly generated benzene sulfinic acid were added and then a few drops of water were added. This reaction mixture was heated at 40°-45° C. for 12 hours and then the benzene was evaporated. The white solid residue obtained was recrystallized from benzene twice and yielded white crystals, m.p. 157°-158° C. The yield was about 88%.

後処理

  1. dissolutionwere dissolved in 250 ml
  2. temperatureThis reaction mixture was heated at 40°-45° C. for 12 hours
  3. customthe benzene was evaporated
  4. customThe white solid residue obtained
  5. customwas recrystallized from benzene twice
  6. customyielded white crystals, m.p. 157°-158° C

出典と根拠

ORDレコード
ord-913d1322b7d14de4aa470eee16f6e226
出典データセット
uspto-grants-1979_11
特許番号
US04174457

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