Hydrochloric Acid → Ethyl 5-[5-(3-phenylpropyl)thiophen-2-yl]pentanoate
Reaction equation
[C:1]1([CH2:7][CH2:8][CH2:9][C:10]2[S:14][C:13]([CH2:15][CH2:16][CH2:17][CH2:18][C:19]([OH:21])=[O:20])=[CH:12][CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl.[CH2:23](O)[CH3:24]>>[C:1]1([CH2:7][CH2:8][CH2:9][C:10]2[S:14][C:13]([CH2:15][CH2:16][CH2:17][CH2:18][C:19]([O:21][CH2:23][CH3:24])=[O:20])=[CH:12][CH:11]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
4
Procedure
3 g of 5-[5-(3-phenylpropyl)-thien-2-yl]-valeric acid are dissolved in 10 ml of ethanol and the solution is saturated with HCl gas. The solution is stirred at room temperature for 24 hours and concentrated in vacuo. Purification by column chromatography (silica gel/hexane/ethyl acetate).
Workup
- concentrationconcentrated in vacuo
- customPurification by column chromatography (silica gel/hexane/ethyl acetate)
Sources & evidence
- ORD record
- ord-0fcece9982ff482b8168ceb731d814e4
- Source dataset
- uspto-grants-1987_11
- Patent number
- US04705802
Reaction notes
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