Hydrochloric Acid → HCID 20088026, compound
Reaction equation
[CH3:1][C:2]([C:5]1[CH:10]=[C:9]([S:11][C@@H:12]2[CH2:16][CH2:15][CH2:14][C@H:13]2O)[CH:8]=[C:7]([C:18]([CH3:21])([CH3:20])[CH3:19])[C:6]=1[OH:22])([CH3:4])[CH3:3].[ClH:23]>>[Cl:23][CH:13]1[CH2:14][CH2:15][CH2:16][CH:12]1[S:11][C:9]1[CH:10]=[C:5]([C:2]([CH3:4])([CH3:3])[CH3:1])[C:6]([OH:22])=[C:7]([C:18]([CH3:21])([CH3:20])[CH3:19])[CH:8]=1Participants
3
Procedure
The product of Example 7 (0.40 g, 0.0012 mole) was stirred with concentrated hydrochloric acid (5 ml) at room temperature for 20 hours. The solid was removed by filtration, washed with water and air dried to give the product as a white powder. The product was purified by silica gel chromatography to give a white solid. The structure was supported by NMR.
Workup
- customThe solid was removed by filtration
- washwashed with water and air
- customdried
Sources & evidence
- ORD record
- ord-be83eb6548484f64b87066365f5ec566
- Source dataset
- uspto-grants-1994_08
- Patent number
- US05334616
Reaction notes
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