Carbon Tetrachloride → HCID 14477024, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH:14]([CH3:16])[CH3:15])[O:9][C:8]([CH3:18])([CH3:17])[CH2:7]C2=O.P(Cl)(Cl)(Cl)(Cl)[Cl:21].[C:26]([Cl:30])(Cl)(Cl)Cl>>[Cl:21][C:7]1[C:8]([CH3:18])([CH3:17])[O:9][C:10]2[C:5]([C:26]=1[Cl:30])=[CH:4][C:3]([O:2][CH3:1])=[C:12]([O:13][CH:14]([CH3:16])[CH3:15])[CH:11]=2Participants
4
Conditions
- Temperature
- 30 °C
Procedure
A suspension of 2.64 g (10 millimoles) of 6-methoxy-7-isopropoxy-2,2-dimethyl-4-chromanone, 4.2 g (20 millimoles) of phosphorous pentachloride and 30 ml of carbon tetrachloride is stirred at 30° C. for 8 hours. The reaction mixture is evaporated and the residue is purified by crystallization from ethanol. Thus 3.8 g of the desired compound are obtained. Yield 60%. Mp.: 80°-85° C.
Workup
- customThe reaction mixture is evaporated
- customthe residue is purified by crystallization from ethanol
Sources & evidence
- ORD record
- ord-51ea225eef6c4ed7bdb015aa520f319a
- Source dataset
- uspto-grants-1987_12
- Patent number
- US04716238
Reaction notes
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