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ChemicalBook CAS DataBase List bicyclo[2.2.1]heptan-4-ol

bicyclo[2.2.1]heptan-4-ol synthesis

12synthesis methods
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Yield:51566-98-4 40%

Reaction Conditions:

Stage #1: norbornenewith oxygen;nitric acid;trifluoroacetic acid at 45 - 50; for 4 h;
Stage #2: with potassium hydroxide in ethanol; for 1 h;

Steps:



Bicyclo[2,2,1]heptane (10.0 g, 104.0 mmol) and trifluoroacetic acid (100 mL) were added to a 250 mL round bottom flask.Concentrated nitric acid (0.3g) was added under stirring.Warming up to 45 to 50 ° C,Stir for 4 hours in an air atmosphere;The trifluoroacetic acid was removed under reduced pressure.A 10% potassium hydroxide ethanol solution (90 mL) was added to the remaining mixture.Stir for 1 hour;Ethanol was removed under reduced pressure, dichloromethane was added to the mixture, washed twice with water and dried over anhydrous magnesium sulfate. Purification,The white crystalline intermediate 1-A-1 (4.7 g; 40%) was obtained.

References:

CN110183332,2019,A Location in patent:Paragraph 0067; 0068

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