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4-Oxoadamantane-1-carboxylic acid → 4-hydroxyadamantane-1-carboxylic Acid

HRID 1424566
ノート
印刷プレビュー

反応式

HRID 1424566 の反応式
[O:1]=[C:2]1[CH:9]2[CH2:10][C:5]3([C:12]([OH:14])=[O:13])[CH2:6][CH:7]([CH2:11][CH:3]1[CH2:4]3)[CH2:8]2.[BH4-].[Na+]>CO>[OH:1][CH:2]1[CH:9]2[CH2:10][C:5]3([C:12]([OH:14])=[O:13])[CH2:6][CH:7]([CH2:11][CH:3]1[CH2:4]3)[CH2:8]2
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 28425154-Oxoadamantane-1-carboxylic acidHCID 4311764Sodium borohydride

生成物 1

HCID 45525374-hydroxyadamantane-1-carboxylic Acid収率 99.9%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A stirred solution of 4-oxoadamantane-1-carboxylic acid (4.42 g, 22.8 mmol) in MeOH (100 mL) was cooled in an ice bath and NaBH4 tablets (4×1 g, 106 mmol) were added at 15 min intervals. The ice bath was allowed to melt and the mixture was stirred overnight at rt and concentrated under reduced pressure. The residue was diluted with 5% aq HCl (100 mL) and extracted with ether (2×125 mL). The combined ether extracts were dried over MgSO4 and concentrated to give 4-hydroxyadamantane-1-carboxylic acid (4.47 g, quant) as an off-white solid which was used directly.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. concentrationconcentrated under reduced pressure
  2. additionThe residue was diluted with 5% aq HCl (100 mL)
  3. extractionextracted with ether (2×125 mL)
  4. dry with materialThe combined ether extracts were dried over MgSO4
  5. concentrationconcentrated

出典と根拠

ORDレコード
ord-880206f3c6bd4f38833f06fba606d756
出典データセット
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08927715B2

反応ノート

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