Thionyl Chloride → HCID 54019687, compound
Reaction equation
[CH2:1]([O:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:13]=1[C:24]([OH:26])=O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].O=S(Cl)[Cl:29]>>[CH2:1]([O:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:13]=1[C:24]([Cl:29])=[O:26])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]Participants
3
Procedure
20 ml of SOCl2 was added to 4 g (1.13×10-2 mol) of decyloxybiphenylcarboxylic acid, and the mixture was heated at reflux for 3.5 hours. Excessive SOCl2 was evaporated to obtain decyloxybiphenylcarboxylic acid chloride.
Workup
- temperaturethe mixture was heated
- temperatureat reflux for 3.5 hours
- customExcessive SOCl2 was evaporated
Sources & evidence
- ORD record
- ord-28bc16bc3a2c47169a326e4ed35f05e8
- Source dataset
- uspto-grants-1992_05
- Patent number
- US05114613
Reaction notes
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