Formaldehyde → (+-)-Pantolactone
Reaction equation
[CH2:1]=[O:2].[CH:3](=[O:7])[CH:4]([CH3:6])[CH3:5].[C-]#N.[Na+].S(=O)(=O)(O)O.[CH3:16][OH:17]>>[CH3:5][C:4]1([CH3:6])[CH:3]([OH:7])[C:16](=[O:17])[O:2][CH2:1]1Participants
6
Procedure
The same apparatus and process was used as in Example 1 except as follows: The starting product comprised 5.45 l/hr. of formalin (30%), 5.35 l/hr. of isobutyraldehyde, 2.35 l/hr. of methanol, 9.25 l/hr. of NaCN solution and 12 l/hr. of sulfuric acid (46%). The latter was used in the hydrolysis step. The residence time in the circulation reactor was 20 min. The temperature in the same reactor was 5° C. The time for the aftertreatment reaction was 40 min. The temperature in the tubular reactor was 150° C. and the residence time therein was 6 min. There were obtained 7 kg pantolactone of 90% purity. The yield was 76%.
Workup
- customThe latter was used in the hydrolysis step
- customwas 5° C
- customThe time for the aftertreatment reaction
- waitwas 40 min
- customwas 150° C.
- waitthe residence time therein was 6 min
Sources & evidence
- ORD record
- ord-8a138cfc384440fdb18cfbed76b62429
- Source dataset
- uspto-grants-1978_06
- Patent number
- US04095952
Reaction notes
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