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Water → 3-Hydroxyiminocamphor

HRID 1885758
ノート
印刷プレビュー

反応式

HRID 1885758 の反応式
[Na].[N:2](OCCC(C)C)=[O:3].O.[CH3:11][C@:12]12[C:20](=[O:21])[CH2:19][C@H:15]([C:16]1([CH3:18])[CH3:17])[CH2:14][CH2:13]2>C(OCC)C>[OH:3][N:2]=[C:19]1[CH:15]2[C:16]([CH3:17])([CH3:18])[C:12]([CH3:11])([CH2:13][CH2:14]2)[C:20]1=[O:21]
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 8053Isoamyl NitriteHCID 159055D-CamphorHCID 5360545Sodium

生成物 1

HCID 68447213-Hydroxyiminocamphor

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

In 600 ml of dried diethyl ether was dissolved 130 g (0.854 mol) of commercially available D-camphor, and 20.4 g of metallic sodium was added thereto. The solution was kept at 0° C. with stirring, and 123 ml (0.916 mol) of isoamyl nitrite was added thereto to conduct a reaction for 14 hours. After completion of the reaction, 200 ml of water was added to the reaction mixture, and the aqueous layer was separated. To the aqueous layer was added 400 ml of 10% hydrochloric acid, and the solid thus formed was extracted with diethyl ether. The ether layer was dried and concentrated to obtain 51 g of 3-hydroxyiminocamphor.

後処理

  1. additionwas added
  2. customwas kept at 0° C.
  3. customa reaction for 14 hours
  4. additionwas added to the reaction mixture
  5. customthe aqueous layer was separated
  6. additionTo the aqueous layer was added 400 ml of 10% hydrochloric acid
  7. customthe solid thus formed
  8. extractionwas extracted with diethyl ether
  9. dry with materialThe ether layer was dried
  10. concentrationconcentrated

出典と根拠

ORDレコード
ord-bbc06c0a733b42528dbf80318ceaf1c1
出典データセット
uspto-grants-1992_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05146003

反応ノート

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