Thionyl Chloride → 3-(2-Fluorocyclopentyloxy)-4-methoxybenzoyl chloride
Reaction equation
[F:1][CH:2]1[CH2:6][CH2:5][CH2:4][CH:3]1[O:7][C:8]1[CH:9]=[C:10]([CH:14]=[CH:15][C:16]=1[O:17][CH3:18])[C:11](O)=[O:12].S(Cl)([Cl:21])=O>C1(C)C=CC=CC=1>[F:1][CH:2]1[CH2:6][CH2:5][CH2:4][CH:3]1[O:7][C:8]1[CH:9]=[C:10]([CH:14]=[CH:15][C:16]=1[O:17][CH3:18])[C:11]([Cl:21])=[O:12]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
A suspension of 3-(2-fluorocyclopentyloxy)-4-methoxybenzoic acid (0.48 g) in toluene (20 mL) is treated with thionyl chloride (0.34 g) and then is heated at 60° C. for 3 hours, and cooled and evaporated to give 3-(2-fluorocyclopentyl-oxy)-4-methoxybenzoyl chloride.
Workup
- temperaturecooled
- customevaporated
Sources & evidence
- ORD record
- ord-546bbe33d58b4bef9e69285450de212d
- Source dataset
- uspto-grants-2001_07
- Patent number
- US06255326B1
Reaction notes
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