Hydrochloric Acid → 4'-Methoxycarbonyloxy-4-biphenylcarboxylic acid

HRID 651302

反応式

HRID 651302 の反応式
Cl[C:2]([O:4][CH3:5])=[O:3].[OH:6][C:7]1[CH:12]=[CH:11][C:10]([C:13]2[CH:18]=[CH:17][C:16]([C:19]([OH:21])=[O:20])=[CH:15][CH:14]=2)=[CH:9][CH:8]=1.[OH-].[Na+].Cl>O>[CH3:5][O:4][C:2]([O:6][C:7]1[CH:8]=[CH:9][C:10]([C:13]2[CH:18]=[CH:17][C:16]([C:19]([OH:21])=[O:20])=[CH:15][CH:14]=2)=[CH:11][CH:12]=1)=[O:3]

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 6586Methyl chloroformateHCID 14798Sodium HydroxideHCID 3015564'-Hydroxy-4-biphenylcarboxylic acid

生成物 1

HCID 183284084'-Methoxycarbonyloxy-4-biphenylcarboxylic acid

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Methyl chloroformate (12.90 g, 0.137 mol) was added dropwise, over 10 minutes, to a stirred. cooled (5° C.) solution of compound 3 (10.00 g, 0.047 mol) in sodium hydroxide (5.44 g, 0.136 mol) and water (150 ml). During the addition a white precipitate was formed and this stirred mixture was allowed to warm to room temperature overnight. The resultant mixture was carefully acidified (pH 5) with dilute hydrochloric acid and the resultant voluminous white solid was filtered off, washed with water until acid-free and dried (phosphorus pentoxide) in vacuo.

後処理

  1. additionDuring the addition a white precipitate
  2. customwas formed
  3. filtrationthe resultant voluminous white solid was filtered off
  4. washwashed with water until acid-free and
  5. dry with materialdried (phosphorus pentoxide) in vacuo

出典と根拠

ORDレコード
ord-5e64d98b6a214eff8da3ed37482288e7
出典データセット
uspto-grants-2001_08
特許番号
US06278028B1

関連ノート

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