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Hydroxyamine hydrochloride → 2a,3,4,5-tetrahydro-2H-acenaphthylen-1-one oxime

HRID 331229
ノート
印刷プレビュー

反応式

HRID 331229 の反応式
[C:1]1(=O)[C:11]2=[C:12]3[C:7](=[CH:8][CH:9]=[CH:10]2)[CH2:6][CH2:5][CH2:4][CH:3]3[CH2:2]1.Cl.[NH2:15][OH:16].C([O-])(=O)C.[Na+]>O.C1COCC1.CO>[C:1]1(=[N:15][OH:16])[C:11]2=[C:12]3[C:7](=[CH:8][CH:9]=[CH:10]2)[CH2:6][CH2:5][CH2:4][CH:3]3[CH2:2]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 443297Hydroxyamine hydrochlorideHCID 517045Sodium AcetateHCID 128585821,2,2a,3,4,5-Hexahydroacenaphthylen-1-one

生成物 1

HCID 866416292a,3,4,5-tetrahydro-2H-acenaphthylen-1-one oxime収率 101.7%

試薬・触媒・溶媒 3

HCID 887Methanol溶媒HCID 962Water
溶媒
2 回
HCID 8028Tetrahydrofuran溶媒

反応条件

温度
75 °C

実験手順

To a mixture of 2a,3,4,5-tetrahydro-2H-acenaphthylen-1-one (12.2 g, 70.9 mmol), hydroxylamine hydrochloride (7.85 g) and water (90 ml) were slowly added sodium acetate (14.5 g), methanol (120 ml), THF (30 ml) and water (60 ml) with stirring while heating at 75° C., and the mixture was stirred for 2 hr and 40 min. After cooling to room temperature, methanol was evaporated under reduced pressure, and the obtained precipitate was collected by filtration, and washed with water to give 2a,3,4,5-tetrahydro-2H-acenaphthylen-1-one oxime (13.5 g).

後処理

  1. stirringthe mixture was stirred for 2 hr and 40 min
  2. temperatureAfter cooling to room temperature
  3. custommethanol was evaporated under reduced pressure
  4. filtrationthe obtained precipitate was collected by filtration
  5. washwashed with water

出典と根拠

ORDレコード
ord-d9f0fe0bf1ed4ea2863ec399767284be
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08877779B2

反応ノート

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