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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Water → HCID 57736351、化合物

HRID 2261331
ノート
印刷プレビュー

反応式

HRID 2261331 の反応式
F[C:2](F)([C:8]([F:17])([F:16])[C:9]([F:15])([F:14])[C:10]([F:13])([F:12])[F:11])[CH:3]=[C:4](I)[CH2:5][OH:6].[OH2:19].Cl.[NH2:21]O.C(=O)([O-])[O-].[K+].[K+]>C(O)C>[F:14][C:9]([F:15])([C:10]([F:13])([F:12])[F:11])[C:8]([F:17])([F:16])[C:2]1[O:19][N:21]=[C:4]([CH2:5][OH:6])[CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 443297Hydroxyamine hydrochlorideHCID 86631047HCID 86631047、化合物

生成物 1

HCID 57736351HCID 57736351、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

14.94 g of 4,4,5,5,6,6,7,7,7-nonafluoro-2-iodo-2-heptene-1-ol was dissolved in 150 ml of ethanol, and 70 ml of water, 5.17 g of hydroxylamine hydrochloride and 25.67 g of potassium carbonate were then added. The mixture was stirred and heated under reflux for 24 hours. The reaction mixture was concentrated under reduced pressure. After water was added, the residue was extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate, filtered and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 3.53 g of (5-heptafluoropropyl-isoxazol-3-yl)methanol.

後処理

  1. temperatureheated
  2. temperatureunder reflux for 24 hours
  3. concentrationThe reaction mixture was concentrated under reduced pressure
  4. additionAfter water was added
  5. extractionthe residue was extracted with ethyl acetate
  6. washThe organic layer was washed with water
  7. dry with materialdried over anhydrous magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-608d1c8e3d7847f3bf2cdc3ddd200e19
出典データセット
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07846956B2

反応ノート

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