Hydrochloric Acid → HCID 21543498, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([C:11]1[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=1)[CH:6]=[C:5]2[CH2:18]C(C1OCCO1)C.Cl.[CH2:27]([OH:29])[CH3:28]>>[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([C:11]1[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=1)[CH:6]=[C:5]2[CH2:18][C:27](=[O:29])[CH3:28]Participants
4
Procedure
A mixture of 14g of 5-chloro-3-[2(1,3-dioxolan-2-yl)propyl]-1-(4-fluorophenyl)indole, 112 ml of 96% ethyl alcohol, and 12 ml of 6N hydrochloric acid are heated to reflux for 30 minutes. The reaction mixture is concentrated then dissolved in water and extracted with ether. The organic phase is washed in water, dried, concentrated and then distilled.
Workup
- temperatureare heated
- temperatureto reflux for 30 minutes
- concentrationThe reaction mixture is concentrated
- dissolutionthen dissolved in water
- extractionextracted with ether
- washThe organic phase is washed in water
- customdried
- concentrationconcentrated
- distillationdistilled
Sources & evidence
- ORD record
- ord-1ad902a9a1b043acb89abe5ffaa74d42
- Source dataset
- uspto-grants-1976_04
- Patent number
- US03953442
Reaction notes
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