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

HRID 1424566
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HRID 1424566 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 28425154-Oxoadamantane-1-carboxylic acidHCID 4311764Sodium borohydride

생성물 1

HCID 45525374-hydroxyadamantane-1-carboxylic Acid수율 99.9%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

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.

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후처리

  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

출처 및 근거

ORD 기록
ord-880206f3c6bd4f38833f06fba606d756
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08927715B2

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