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Idramantone → 5-Hydroxy-adamantan-2-one oxime

HRID 12816
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HRID 12816 반응식
[OH:1][C:2]12[CH2:11][CH:6]3[CH2:7][CH:8]([CH2:10][CH:4]([C:5]3=O)[CH2:3]1)[CH2:9]2.Cl.[NH2:14][OH:15]>CCO.[OH-].[Na+]>[OH:1][C:2]12[CH2:11][CH:6]3[CH2:7][CH:8]([CH2:10][CH:4]([C:5]3=[N:14][OH:15])[CH2:3]1)[CH2:9]2
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참가 물질

5

반응물 2

HCID 64184IdramantoneHCID 443297Hydroxyamine hydrochloride

생성물 1

HCID 230089835-Hydroxy-adamantan-2-one oxime수율 73.4%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 14798Sodium Hydroxide용매

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온도
100 °C

실험 절차

5-Hydroxy-2-admantanone (15 g, 90.2 mmol, CAS #: 20098-14-0, purchased from TCI) was dissolved in EtOH (100 mL) and added to a solution of hydroxylamine hydrochloride (10 g, 143.9 mmol) in 1N NaOH (80 mL). The mixture was heated at 100° C. for 2 hours. The EtOH was evaporated, and water and dichloromethane were added. The resulting mixture was stirred for 10 min and then filtered. The solid was collected. The resulting mixture was separated. The aqueous layer was further extracted twice with dichloromethane. The combined organic phases were concentrated under high vacuum. The resulting residue was combined with the solid from the filtration. Crystallization from EtOAc gave 5-hydroxy-adamantan-2-one oxime (12 g, 73%). Mass spectrum: m/z: 182 (M+1).

후처리

  1. customThe EtOH was evaporated
  2. additionwater and dichloromethane were added
  3. filtrationfiltered
  4. customThe solid was collected
  5. customThe resulting mixture was separated
  6. extractionThe aqueous layer was further extracted twice with dichloromethane
  7. concentrationThe combined organic phases were concentrated under high vacuum
  8. filtrationThe resulting residue was combined with the solid from the filtration
  9. customCrystallization from EtOAc

출처 및 근거

ORD 기록
ord-c831c44eb924457a978b16137d236615
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07728029B2

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