1,4-Dioxane hydrochloride → HCID 86643129, compound
Reaction equation
Cl.O1CCOCC1.[CH3:8][N:9]([CH3:25])[C:10](=[S:24])[S:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([O:18][CH3:19])[C:13]=1[O:20]COC>CO>[CH3:25][N:9]([CH3:8])[C:10](=[S:24])[S:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([O:18][CH3:19])[C:13]=1[OH:20]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4 N hydrogen chloride/dioxane solution (50 mL) was added to a methanol (200 mL) solution of the compound (70.49 g) synthesized in the above (2), and stirred at room temperature for 2 hours. The reaction liquid was concentrated and extracted with chloroform. The organic layer was washed with saturated saline, then dried with sodium sulfate, and concentrated to obtain the intended compound (46.65 g, 78%) as a brown solid.
Workup
- customThe reaction liquid
- concentrationwas concentrated
- extractionextracted with chloroform
- washThe organic layer was washed with saturated saline
- dry with materialdried with sodium sulfate
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-57d13a18444c467284999d559e082f2e
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08163770B2
Reaction notes
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