Reaction equation
[C:1]1([C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4])[OH:2].[P:9](Cl)(Cl)([O:11][CH3:12])=[O:10].C(#N)C>C(N(CC)CC)C>[P:9]1([O:4][C:3]2[CH:5]=[CH:6][CH:7]=[CH:8][C:1]=2[O:2]1)([O:11][CH3:12])=[O:10]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- -25 °C
Procedure
To 1.418 g of pyrocatechol were added 1.917 g of methyl dichlorophosphate and 11 ml of acetonitrile. The mixture was cooled to -25° C. and 2.605 g of triethylamine was added dropwise at -25° C. to -20° C. with stirring. The dropping funnel was washed with 1 ml of acetonitrile and the washings were added to the mixture. After stirring at the same temperature for 10 minutes, the reaction mixture was allowed to return to 10° C. and then filtered. The filtration residue was washed with a 5-ml and 3-ml portion of acetonitrile. The filtrate and washings were concentrated under reduced pressure on a water bath at 15° C. to 20° C. to give 3.102 g of methyl o-phenylene phosphate as a slightly turbid oil.
Workup
- washThe dropping funnel was washed with 1 ml of acetonitrile
- additionthe washings were added to the mixture
- stirringAfter stirring at the same temperature for 10 minutes
- customto return to 10° C.
- filtrationfiltered
- washThe filtration residue was washed with a 5-ml and 3-ml portion of acetonitrile
- concentrationThe filtrate and washings were concentrated under reduced pressure on a water bath at 15° C. to 20° C.
Sources & evidence
- ORD record
- ord-d77a62d525934f06b2125385bee352a7
- Source dataset
- uspto-grants-1987_02
- Patent number
- US04642365
Linked notes
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