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Lithium Hydroxide → HCID 74943869、化合物

HRID 2427930
ノート
印刷プレビュー

反応式

HRID 2427930 の反応式
[CH3:1][C:2]([CH3:8])([CH3:7])[C:3](=[N:5][OH:6])[CH3:4].[Li+].[OH-].[CH2:11]1[O:13][CH2:12]1>O>[OH:13][CH2:12][CH2:11][O:6][N:5]=[C:3]([C:2]([CH3:8])([CH3:7])[CH3:1])[CH3:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 3939Lithium HydroxideHCID 6354Ethylene OxideHCID 137609N-(3,3-Dimethylbutan-2-ylidene)hydroxylamine

生成物 1

HCID 74943869HCID 74943869、化合物収率 90%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

400 ml of water, 92 g (0.8 mol) of 3,3-dimethylbutan-2-one oxime and 3.4 g of LiOH were initially charged, and 70 g (1.6 mol) of ethylene oxide were introduced such that the gas was taken up completely. Thereafter, the mixture was stirred at room temperature (RT) for 8-12 hours for the continued reaction. The upper phase was removed, admixed with ethyl acetate and washed with water. The organic phase was concentrated under reduced pressure at 100-200 mbar. Residue: 114-120 g of colorless oil, which corresponds to a yield of 90% yield; b.p. 106° C./35 mbar.

後処理

  1. customfor the continued reaction
  2. customThe upper phase was removed
  3. washwashed with water
  4. concentrationThe organic phase was concentrated under reduced pressure at 100-200 mbar

出典と根拠

ORDレコード
ord-01bef4b727d14d56b3db211d3f892815
出典データセット
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07968747B2

反応ノート

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