Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Propanediol | HCID 10442 | — |
| Reactant | 2-Propyl-1,3-dioxane | HCID 283981 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 1,3-Propanediol | HCID 10442 | — |
| Product | 2-Propyl-1,3-dioxane | HCID 283981 | — |
| Product | HCID 13419439 | HCID 13419439 | — |
Reaction Steps
1000 g of 1,3-propanediol and 500 g of 2-propyl-1,3-dioxane were combined in a 2 L stainless steel autoclave with 6.0 g of 5% Pd on carbon catalyst. The reactor was sealed and purged twice with N2 and once with H2. The reactor was charged with H2 and heated to 200° C. The reactor was brought to an operating pressure of 6.89 MPa and stirring commenced at 750 rpm. Temperature and pressure were maintained for 2 h. The reactor was cooled, vented, and the contents filtered. The filtrate was analyzed by GC to yield 153 g of 2-propyl-1,3-dioxane, 288 g of 3-BP, 15.9 g of 1,3-dibutoxypropane, and 1017 g of 1,3-propanediol. This corresponds to yield 69% conversion of the acetal and 95% selectivity to the desired ether alcohol, 3-BP.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09388105B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-df459c7bad0e4925a61e615aa30717ba |
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| Source note | uspto-grants-2016_07 |
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