Hydrochloric Acid → 6328-86-5
Reaction equation
Br[CH2:2][C:3]1[O:8][C:7](=[O:9])[CH:6]=[C:5]([OH:10])[CH:4]=1.Cl.[OH-:12].[Na+]>O>[OH:10][C:5]1[CH:4]=[C:3]([CH2:2][OH:12])[O:8][C:7](=[O:9])[CH:6]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 50 °C
Procedure
6-Bromomethyl-4-hydroxypyran-2-one (21.1 parts) was dissolved in a solution of sodium hydroxide (4.1 parts) in water (800 parts) at 20°-25° C. This solution was added over about 2 hours to a solution of sodium hydroxide (34.2 parts) in water (3200 parts) at 50° C.±3° C. The mixture was stirred for a further hour at 50° C. before acidifying with 35% hydrochloric acid and distilling off the bulk of the water at 50° C./20 mm. The mixture was cooled to 20° C. and insoluble material was filtered off. The filtrate was saturated with sodium chloride and then extracted with ethyl acetate (15×125 parts). The combined extracts were dried over magnesium sulphate and the solvent removed at 40° C./20 mm to give 4-hydroxy-6-hydroxymethylpyran-2-one (10.2 parts, 69%).
Workup
- distillationdistilling off the bulk of the water at 50° C./20 mm
- temperatureThe mixture was cooled to 20° C.
- filtrationinsoluble material was filtered off
- extractionextracted with ethyl acetate (15×125 parts)
- dry with materialThe combined extracts were dried over magnesium sulphate
- customthe solvent removed at 40° C./20 mm
Sources & evidence
- ORD record
- ord-111d9c490bd64c338a63bca79d24b43f
- Source dataset
- uspto-grants-1995_08
- Patent number
- US05443970
Reaction notes
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