Lithium Chloride → Cyclohexadecanone
Reaction equation
[O:1]1[CH:3]2[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH:2]12.[Cl-].[Li+]>CN1CCCC1=O>[C:2]1(=[O:1])[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 200 °C
Procedure
A mixture containing 10.5 g of epoxy-cyclohexadecane, 10 g of N-methylpyrrolidone, and 0.5 g of lithium chloride was stirred at 200° C. for 6 hours. With a 100% conversion, a 98.9% yield of cyclohexadecanone was obtained.
Sources & evidence
- ORD record
- ord-347fa5dd23b648d6ab30a23638a4a096
- Source dataset
- uspto-grants-1989_12
- Patent number
- US04885397
Reaction notes
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