p-Acetoxybenzoyl chloride → HCID 10862141, compound
Reaction equation
[C:1]([O:4][C:5]1[CH:13]=[CH:12][C:8]([C:9](Cl)=[O:10])=[CH:7][CH:6]=1)(=[O:3])[CH3:2].[Cl-].[Al+3].[Cl-].[Cl-].[CH:18]1[CH:19]=[C:20]([CH2:27][CH2:28][CH2:29][C:30]([O:32][CH2:33][CH3:34])=[O:31])[N:21]2[C:26]=1[CH:25]=[CH:24][CH:23]=[CH:22]2>ClCCl>[C:1]([O:4][C:5]1[CH:13]=[CH:12][C:8]([C:9]([C:18]2[CH:19]=[C:20]([CH2:27][CH2:28][CH2:29][C:30]([O:32][CH2:33][CH3:34])=[O:31])[N:21]3[C:26]=2[CH:25]=[CH:24][CH:23]=[CH:22]3)=[O:10])=[CH:7][CH:6]=1)(=[O:3])[CH3:2]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
4-Acetoxybenzoyl chloride (53.6 g) was added to a suspension of aluminum chloride (36.5 g) in dichloromethane (500 ml). After the mixture was stirred for 20 minutes at room temperature, a solution of ethyl 4-(indolizin-3-yl)butyrate (57.8 g) in dichloromethane (50 ml) was added to the mixture. The mixture was stirred for 2 hours at room temperature and the solvent was evaporated. The residue was dissolved in ethyl acetate (500 ml) and washed with water. N,N-dimethylaminopropylamine (20 ml) was added to the solution. The mixture was washed with diluted hydrochloric acid, water, sodium bicarbonate aqueous solution and water. The solution was dried over magnesium sulfate and the solvent was removed in vacuo. The residue was washed with diisopropyl ether to give ethyl 4-[1-(4-acetoxybenzoyl)indolizin-3-yl]butyrate as yellow powder (36.5 g).
Workup
- stirringThe mixture was stirred for 2 hours at room temperature
- customthe solvent was evaporated
- dissolutionThe residue was dissolved in ethyl acetate (500 ml)
- washwashed with water
- additionN,N-dimethylaminopropylamine (20 ml) was added to the solution
- washThe mixture was washed with diluted hydrochloric acid, water, sodium bicarbonate aqueous solution and water
- dry with materialThe solution was dried over magnesium sulfate
- customthe solvent was removed in vacuo
- washThe residue was washed with diisopropyl ether
Sources & evidence
- ORD record
- ord-bfa7df34696440778d928ef93ef90127
- Source dataset
- uspto-grants-1994_08
- Patent number
- US05334716
Reaction notes
Loading…