Water → HCID 13086534, compound
Reaction equation
[CH3:1][C:2]12[CH2:11][CH:6]3[CH2:7][CH:8]([CH2:10][C:4]([OH:12])([CH2:5]3)[CH2:3]1)[CH2:9]2.[C:13](OC(=O)C)(=[O:15])[CH3:14].S(=O)(=O)(O)O.O.C(=O)(O)[O-].[Na+]>CCCCCCC.C1CCCCC1.CCOCC>[C:13]([O:12][C:4]12[CH2:5][CH:6]3[CH2:7][CH:8]([CH2:9][C:2]([CH3:1])([CH2:11]3)[CH2:3]1)[CH2:10]2)(=[O:15])[CH3:14]Participants
9
Procedure
121 mg (0.728 mmoles) of 3-methyl-1-adamantanol are dissolved in 0.2 mL n-heptane and 0.2 mL cyclohexane. A mixture of 0.2 mL (2.25 mmoles) of acetic anhydride and 2 microliters (0.036 mmoles) of concentrated sulfuric acid is added, and the mixture is at ambient temperature for 20.5 hours. The solution is dissolved in 10 L of ether and extracted with 10 mL of water. The aqueous layer is extracted with 10 mL ether. The ether layers are combined, extracted with 2×mL of water followed by 40 mL of aqueous sodium bicarbonate (10 g/liter), dried over magnesium sulfate, and stripped of solvent in vacuo. The product is a colorless oil with Rf 0.55 (silica: eluant hexane 75%, ethyl acetate 25%).
Workup
- additionis added
- extractionextracted with 10 mL of water
- extractionThe aqueous layer is extracted with 10 mL ether
- dry with materialdried over magnesium sulfate
Sources & evidence
- ORD record
- ord-23dee9fbdebb4e60a3d63ced5fa5ffbe
- Source dataset
- uspto-grants-2004_11
- Patent number
- US06825226B2
Reaction notes
Loading…