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Sodium Hydroxide → 2-(4-Chloro-6-fluoro-1-hydroxy-1-indanyl)acetic acid

HRID 726148
ノート
印刷プレビュー

反応式

HRID 726148 の反応式
[Cl:1][C:2]1[CH:10]=[C:9]([F:11])[CH:8]=[C:7]2[C:3]=1[CH2:4][CH2:5][C:6]2([CH2:13][C:14]([O:16]CC)=[O:15])[OH:12].[OH-].[Na+]>C(O)C>[Cl:1][C:2]1[CH:10]=[C:9]([F:11])[CH:8]=[C:7]2[C:3]=1[CH2:4][CH2:5][C:6]2([CH2:13][C:14]([OH:16])=[O:15])[OH:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 14798Sodium HydroxideHCID 10978626Ethyl 2-(4-chloro-6-fluoro-1-hydroxy-1-indanyl)acetate

生成物 1

HCID 110860282-(4-Chloro-6-fluoro-1-hydroxy-1-indanyl)acetic acid収率 102.2%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A mixture of ethyl 2-(4-chloro-6-fluoro-1-hydroxy-1-indanyl)acetate (14.5 g, 0.05 mol), 1N sodium hydroxide (52 ml) and absolute ethanol (100 ml) was stirred for 18 h at room temperature. The mixture was concentrated in vacuo, diluted with H2O and washed with diethyl ether. The aqueous phase was neutralised with 1.0N hydrochloric acid (52 ml) and extracted with diethyl ether. The diethyl ether extracts were dried over sodium sulphate, filtered and concentrated in vacuo to give 12.5 g (96%) of crude 2-(4-chloro-6-fluoro-1-hydroxy-1-indanyl)acetic acid. This material was used immediately without further purification.

後処理

  1. concentrationThe mixture was concentrated in vacuo
  2. additiondiluted with H2O
  3. washwashed with diethyl ether
  4. extractionextracted with diethyl ether
  5. dry with materialThe diethyl ether extracts were dried over sodium sulphate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-c54cfe93aee64559ac7ef51915a84c96
出典データセット
uspto-grants-1998_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05708033

反応ノート

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