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Hydrochloric Acid → HCID 20511955、化合物

HRID 1089615
ノート
印刷プレビュー

反応式

HRID 1089615 の反応式
C[C:2]1[C:7]2[CH:8]=[CH:9][O:10][C:6]=2[CH:5]=[CH:4][C:3]=1C=O.ClC1C(C(OO)=[O:21])=CC=CC=1.[OH-].[Na+].Cl.[Na+].[Cl-]>C(Cl)Cl.C(OCC)(=O)C>[O:10]1[C:6]2[CH:5]=[CH:4][CH:3]=[CH:2][C:7]=2[CH2:8][CH:9]1[OH:21]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 313Hydrochloric AcidHCID 5234Sodium ChlorideHCID 14798Sodium HydroxideHCID 125873982-Chlorobenzene-1-carboperoxoic acidHCID 144849494-Methylbenzofuran-5-carbaldehyde

生成物 1

HCID 20511955HCID 20511955、化合物

試薬・触媒・溶媒 2

HCID 6344
Dichloromethane
溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

To a solution of 34 (33.06 g, 206 mmol) in methylene chloride (580 mL) was added 80% m chloroperbenzoic acid (52.0 g, 211 mmol) and the mixture heated at reflux for 17 hours. The reaction mixture was allowed to cool, diluted with ethyl acetate (580 mL) and extracted with 5% NaHCO3 (2×725 mL). The aqueous layers were back extracted with additional portions of ethyl acetate (290 mL) and the combined organic layers dried (MgSO4) and concentrated. The resulting yellow oil (47 ) was taken up in methanol (700 mL) and 2.5N NaOH (185 mL, 462 mmol) was added. The mixture was stirred at room temperature for 20 minutes, cooled with an ice bath, and acidified with 2N HCl (810 mL). The resulting mixture was saturated with NaCl and extracted with ethyl acetate (3×1200 mL). The combined extracts were washed with 20% NaCl (2×900 mL), dried (MgSO 4) and concentrated. The resulting dark oil (51 g) was chromatographed through a large (9 cm diameter) column of flash silica gel. Elution with 12.5% ethyl acetate in hexane afforded 36 as an off white solid.

後処理

  1. temperaturethe mixture heated
  2. temperatureat reflux for 17 hours
  3. temperatureto cool
  4. extractionextracted with 5% NaHCO3 (2×725 mL)
  5. extractionThe aqueous layers were back extracted with additional portions of ethyl acetate (290 mL)
  6. dry with materialthe combined organic layers dried (MgSO4)
  7. concentrationconcentrated
  8. temperaturecooled with an ice bath
  9. extractionextracted with ethyl acetate (3×1200 mL)
  10. washThe combined extracts were washed with 20% NaCl (2×900 mL)
  11. dry with materialdried (MgSO 4)
  12. concentrationconcentrated
  13. customThe resulting dark oil (51 g) was chromatographed through a large (9 cm diameter) column of flash silica gel
  14. washElution with 12.5% ethyl acetate in hexane

出典と根拠

ORDレコード
ord-50de9d8ef56e48cdb5c0d02db305b85e
出典データセット
uspto-grants-1990_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04966907

反応ノート

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