Thionyl Chloride → HCID 15045079, compound
Reaction equation
[CH3:1][C:2]1[C:14]2[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[CH:7]([CH2:15][CH2:16][C:17]([OH:19])=O)[C:6]=2[CH:5]=[CH:4][CH:3]=1.O=S(Cl)[Cl:22]>CO.O>[CH3:1][C:2]1[C:14]2[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[CH:7]([CH2:15][CH2:16][C:17]([Cl:22])=[O:19])[C:6]=2[CH:5]=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
3-(4-Methylfluoren-9-yl)propionic acid (3.5 g, 13 9 mmol) was charged with SOCl2 (20 mL, in excess) at room temperature. The reaction mixture was boiled for 2 hr. The reaction was monitored by TLC (silica RP-18, 70% methanol/water). The excess of thionyl chloride was removed under reduced pressure, the residue (an oil) was used for the next step without further purification.
Workup
- customThe excess of thionyl chloride was removed under reduced pressure
- customthe residue (an oil) was used for the next step without further purification
Sources & evidence
- ORD record
- ord-9c8f10c0a87742fbb726342f4032061f
- Source dataset
- uspto-grants-1992_01
- Patent number
- US05079260
Reaction notes
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