Sulfuric Acid → HCID 53938834, compound
Reaction equation
[O:1]([CH2:14][CH3:15])[C@@H:2]1[O:10][C@H:9]([C:11]([O-:13])=[O:12])[C@H:7]([OH:8])[C@H:5]([OH:6])[C@H:3]1[OH:4].[Na+].S(=O)(=O)(O)O>O>[O:1]([CH2:14][CH3:15])[C@@H:2]1[O:10][C@H:9]([C:11]([OH:13])=[O:12])[C@H:7]([OH:8])[C@H:5]([OH:6])[C@H:3]1[OH:4]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
100 g (0.4 mol) of sodium ethyl β-D-galactopyranoside uronate prepared according to Example No. 10 is solubilized in water (20% solution). After adding sulphuric acid up to pH=2, concentrating under vacuum and selectively precipitating the salts in acetone, ethyl β-D-galactopyranoside uronic acid is recovered with a 90% yield (80 grams). Its physicochemical characteristics are given below:
Workup
- concentrationconcentrating under vacuum
- customselectively precipitating the salts in acetone
- customethyl β-D-galactopyranoside uronic acid is recovered with a 90% yield (80 grams)
Sources & evidence
- ORD record
- ord-912bbf1932ca480a98a27bde84c23550
- Source dataset
- uspto-grants-1997_11
- Patent number
- US05688929
Reaction notes
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