Hydrochloric Acid → HCID 12052987, compound
Reaction equation
[CH3:1][CH:2]([CH2:8][C:9]1[N:10]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:11]=[CH:12][CH:13]=1)[C:3]([O:5]CC)=[O:4].Cl>CCOCC>[CH3:1][CH:2]([CH2:8][C:9]1[N:10]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:11]=[CH:12][CH:13]=1)[C:3]([OH:5])=[O:4]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 92.5 °C
Procedure
A mixture of ethyl 2-methyl-3-[1-phenylpyrrol-2-yl]propanoate (0.164 mol, 42.1 g) and Claisen's reagent (78 ml) were heated at 90-95° C. for 1 h. After cooling to room temperature, the solution was diluted with 75 g of crushed ice and acidified to pH 1-2 with 6 N HCl. The brown oily precipitate was dissolved in ether, washed with brine solution, dried over MgSO4, and evaporated to an orange oil (21.65 g). The title compound was analysed by 1H-NMR spectroscopy.
Workup
- temperatureAfter cooling to room temperature
- washwashed with brine solution
- dry with materialdried over MgSO4
- customevaporated to an orange oil (21.65 g)
Sources & evidence
- ORD record
- ord-f1da112343894530bb30c71555bc4e26
- Source dataset
- uspto-grants-2002_09
- Patent number
- US06444833B1
Reaction notes
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