Reaction equation
[CH2:1]([OH:14])[CH:2]([OH:13])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].C1(C)C=CC=CC=1.[B:22]([OH:25])([OH:24])[OH:23]>O>[B:22]([OH:25])([OH:24])[OH:23].[CH2:1]([OH:14])[CH:2]([OH:13])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 75 °C
Procedure
Approximately 151 g of 1,2-dodecanediol and 150 g of toluene were charged to a 1 liter reactor equipped with agitator, heater and Dean-Stark tube with condenser and provision for using a nitrogen vapor space blanket. The contents were heated up to 75° C., and 45 g of boric acid was added. The mixture was heated up to 155° C. over a period of 5 hours until water evolution stopped. The solvent was removed by vacuum distillation and the product was filtered hot through diatomaceous earth. The product was a viscous, clear yellow fluid.
Workup
- customequipped with agitator, heater and Dean-Stark tube with condenser
- customThe solvent was removed by vacuum distillation
- filtrationthe product was filtered hot through diatomaceous earth
Sources & evidence
- ORD record
- ord-33cb7a4021754a4e91a30975ef1b1bee
- Source dataset
- uspto-grants-1988_11
- Patent number
- US04788340
Linked notes
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