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9-Benzyl-3-oxa-9-azabicyclo(3.3.1)nonan-7-one → 3-Oxa-9-azabicyclo[3.3.1]nonan-7-one

HRID 1393202
ノート
印刷プレビュー

反応式

HRID 1393202 の反応式
C([N:8]1[CH:13]2[CH2:14][C:15](=[O:17])[CH2:16][CH:9]1[CH2:10][O:11][CH2:12]2)C1C=CC=CC=1>CCOC(C)=O.CC(O)=O.[Pd]>[CH:9]12[NH:8][CH:13]([CH2:14][C:15](=[O:17])[CH2:16]1)[CH2:12][O:11][CH2:10]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 1

HCID 156391149-Benzyl-3-oxa-9-azabicyclo(3.3.1)nonan-7-one

生成物 1

HCID 552883333-Oxa-9-azabicyclo[3.3.1]nonan-7-one

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 22609514Ethyl acetate acetate溶媒

実験手順

To a stirring mixture of 9-benzyl-3-oxa-9-aza-bicyclo[3.3.1]nonan-7-one (1.1 g, 4.76 mmol) in EtOAc/HOAc (6 mL, 1:1, v/v) was added palladium on carbon (250 mg). The resulting mixture was stirred at room temperature under an atmosphere of hydrogen for 2 days. The suspension was filtered through Celite and the filtrate was concentrated under vacuum to give a quantitative yield of 3-oxa-9-aza-bicyclo[3.3.1]nonan-7-one as a yellow oil. This crude mixture was converted to the corresponding hydrochloric salt by the addition of HCl (3 mL, 1N aqueous HCl). The mixture was concentrated under reduced pressure and this process was repeated twice. Retention time (min)=0.231, Method [1], MS(ESI) 142.2 (M+H).

後処理

  1. filtrationThe suspension was filtered through Celite
  2. concentrationthe filtrate was concentrated under vacuum

出典と根拠

ORDレコード
ord-170c5bf807f74809b9383a612f50339d
出典データセット
uspto-grants-2008_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07345056B2

反応ノート

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