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Hydrochloric Acid → 5-(4-Chlorophenyl)-5-hydroxypentanoic acid

HRID 1904616
ノート
印刷プレビュー

反応式

HRID 1904616 の反応式
[Cl:1][C:2]1[CH:15]=[CH:14][C:5]([C:6]([CH2:8][CH2:9][CH2:10][C:11]([OH:13])=[O:12])=[O:7])=[CH:4][CH:3]=1.[OH-].[Na+].[BH4-].[Na+].Cl>O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH:6]([OH:7])[CH2:8][CH2:9][CH2:10][C:11]([OH:13])=[O:12])=[CH:14][CH:15]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 27337165-(4-Chlorophenyl)-5-oxopentanoic acidHCID 4311764Sodium borohydride

生成物 1

HCID 145768835-(4-Chlorophenyl)-5-hydroxypentanoic acid収率 70.1%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a solution of 10.6 g of 4-(4-chlorobenzoyl)butanoic acid and 1.9 g of sodium hydroxide in 50 ml of water was added under ice-cooling 2.7 g of sodium borohydride portionwise over 35 minutes, and the mixture was stirred at room temperature for 24 hours. The mixture was made acidic with diluted hydrochloric acid under ice-cooling, extracted with ether. The ether extract was washed with water and dried. After removal of the solvent, the residue was recrystallized from a mixture of ethyl acetate-n-hexane to give 7.50 g of 5-(4-chlorophenyl)-5-hydroxypentanoic acid as colorless crystals.

後処理

  1. temperaturecooling
  2. extractionextracted with ether
  3. extractionThe ether extract
  4. washwas washed with water
  5. customdried
  6. customAfter removal of the solvent
  7. customthe residue was recrystallized from a mixture of ethyl acetate-n-hexane

出典と根拠

ORDレコード
ord-5991b39119094401bb1201f1408f526a
出典データセット
uspto-grants-1989_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04839360

反応ノート

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