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2,3-dihydro-3-phenyl-4H-1-benzopyran-4-one → Isoflavan

HRID 2292124
ノート
印刷プレビュー

反応式

HRID 2292124 の反応式
[O:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4](=O)[CH:3]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:2]1>C(O)(=O)C.Cl.[Zn]>[O:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH:3]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:2]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 1

HCID 1607672,3-dihydro-3-phenyl-4H-1-benzopyran-4-one

生成物 1

HCID 500472Isoflavan

試薬・触媒・溶媒 3

HCID 23994Zinc触媒HCID 176Acetic Acid溶媒HCID 313Hydrochloric Acid溶媒

実験手順

Isoflavanone (0.90 g) was dissolved in a mixture of acetic acid (15 ml) and concentrated hydrochloric acid (1.5 ml). and the solution added to zinc amalgam prepared from zinc powder (2.5 g) and mercuric chloride (0.25 g). The mixture was stirred for 45 min., then allowed to stand at room temperature for 18 hrs. The mixture was filtered and the filtrate diluted with water. The precipitated oil was extracted into toluene and the extract washed with saturated sodium hydrogen bicarbonate solution, dried, and evaporated. The residue was chromatographed on alumina, eluting with petroleum ether, (60°-80°) to give, on evaporation of the eluate, pure isoflavan, 0.23 g., m.pt. 54°-56°.

後処理

  1. waitto stand at room temperature for 18 hrs
  2. filtrationThe mixture was filtered
  3. additionthe filtrate diluted with water
  4. extractionThe precipitated oil was extracted into toluene
  5. washthe extract washed with saturated sodium hydrogen bicarbonate solution
  6. customdried
  7. customevaporated
  8. customThe residue was chromatographed on alumina
  9. washeluting with petroleum ether, (60°-80°)

出典と根拠

ORDレコード
ord-9692c5fc4f5f4828b6f8ffba9e4914a1
出典データセット
uspto-grants-1989_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04801593

反応ノート

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