Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butanal | HCID 261 | — |
| Reactant | Propylene Glycol | HCID 1030 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | HCID 131731839 | HCID 131731839 | — |
Reaction Steps
n-Butyraldehyde (3.6 g, 4.5 ml; 0.05 mol), 1,2-propanediol (76.1 g, 73.4 ml; 1 mol), and 0.18 g of 10% Pd/C (5 wt % to n-butyraldehyde) are charged to a 150 ml Parr reactor. The system is purged with nitrogen three times. Then 500 psi of hydrogen is charged, the reactor is heated to 180° C., and the hydrogen pressure is adjusted to 1000 psi. After 3 hours at 180° C. and 1000 psi, GC analysis shows complete conversion of n-butyraldehyde and formation of an approximately 1:1 mixture of 2-butoxy-1-propanol and 1-butoxy-2-propanol (79.2%), n-butanol (5.8%), and cis/trans 2-propyl-4-methyl-1,3-dioxolane (11.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829229B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-b4c185c0de19400b82302d03b7607c44 |
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| Source note | uspto-grants-2014_09 |
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