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Hydrogen Peroxide → (1S,2S,5R)-2-isopropyl-5-methylcyclohexanecarboxamide

HRID 1970194
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HRID 1970194 반응식
[CH:1]([C@@H:4]1[CH2:9][CH2:8][C@@H:7]([CH3:10])[CH2:6][C@@H:5]1[C:11]#[N:12])([CH3:3])[CH3:2].[OH:13]O.[OH-].[Na+]>CS(C)=O.O>[CH:1]([C@@H:4]1[CH2:9][CH2:8][C@@H:7]([CH3:10])[CH2:6][C@@H:5]1[C:11]([NH2:12])=[O:13])([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 784Hydrogen PeroxideHCID 14798Sodium HydroxideHCID 11073771(1S,2S,5R)-Neomenthyl cyanide

생성물 1

HCID 59253418(1S,2S,5R)-2-isopropyl-5-methylcyclohexanecarboxamide

시약·촉매·용매 2

HCID 679Dimethyl Sulfoxide용매HCID 962Water용매

실험 절차

A solution of 0.105 g (0.634 mmol) of (1S,2S,5R)-2-isopropyl-5-methylcyclohexanecarbonitrile in 4.9 mL of dimethyl sulfoxide was placed in a 10 mL flask with a magnetic stir bar. After adding 0.60 mL of 35% hydrogen peroxide and 0.097 g (1.2 mmol) of 50% sodium hydroxide solutions the flask was capped and stirred at room temperature for 20 h. The reaction mixture was diluted with 10 mL of water, extracted twice with 10 mL of methylene chloride. The combined methylene chloride layers were back extracted with 3×20 mL of water, dried over magnesium sulfate, and concentrated in vacuo to provide an off-white solid that was further purified by column chromatography (silica gel, 75:25 hexane:ethyl acetate) to provide (1S,2S,5R)-2-isopropyl-5-methylcyclohexanecarboxamide.

후처리

  1. customwas capped
  2. extractionextracted twice with 10 mL of methylene chloride
  3. extractionThe combined methylene chloride layers were back extracted with 3×20 mL of water
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated in vacuo
  6. customto provide an off-white solid
  7. customthat was further purified by column chromatography (silica gel, 75:25 hexane:ethyl acetate)

출처 및 근거

ORD 기록
ord-d0a756228eda4eb486d1c59b908cab25
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08426643B2

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