Trimethyl Phosphate → HCID 178502936, compound
Reaction equation
[Cl-].[C:2]1([I+:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[P:15](OC)([O:19][CH3:20])([O:17][CH3:18])=[O:16]>>[CH3:18][O:17][PH:15](=[O:16])[O:19][CH3:20].[C:9]1([I+:8][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=1Participants
3
Procedure
Diphenyliodonium chloride (315 mg; 1 mmol) and trimethyl phosphate (1 g) were stirred at 170° C. for 10 minutes. After the reactants were dissolved, the mixture was cooled, to thereby yield solid matter. The solid matter was washed with ether, to thereby yield 250 mg of the target compound as white crystals (yield: 81.6%). The anion content of the resultant compound was determined by ion chromatography. The chloride anion content was determined to be not greater than 10 ppm.
Workup
- dissolutionAfter the reactants were dissolved
- temperaturethe mixture was cooled
- customto thereby yield solid matter
- washThe solid matter was washed with ether
Sources & evidence
- ORD record
- ord-3964f1b467fd450cb3afcb2aab13d4d5
- Source dataset
- uspto-grants-2003_09
- Patent number
- US06620957B1
Reaction notes
Loading…