HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904440Generated: October 26, 2026
Methanol → 1,1,1-Trifluoro-3,3-dimethoxypropane
https://huagongshe.com/reaction/1904440
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | 3,3,3-Trifluoropropene | HCID 12672 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Catalyst | HCID 178526209 | HCID 178526209 | — |
| Product | 1,1,1-Trifluoro-3,3-dimethoxypropane | HCID 2782445 | — |
Reaction Steps
In a glass autoclave, a mixture of 150 g (4.69 mol) of methanol, 150 g of 1,4-dioxane, 3.0 g (0.017 mol) of PdCl2, 5.8 g (0.034 mol) of CuCl2.2H2O and 4.0 g of Al(OH)3 was kept heated at 60° C. Stirring the mixture, 3,3,3-trifluoropropene was continuously introduced into the autoclave so as to keep the gas pressure in the autoclave at 8 kg/cm2. This operation was continued for 10 hr. As the result 245.2 g (1.552 mol) of 1,1-dimethoxy-3,3,3-trifluoropropane was obtained. In this case selectivity to this acetal was 60.2%, and the remaining part of the reaction product was 3,3,3-trifluoropropanal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04837366 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-b9947dac74834b989c2e9368fe575c64 |
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| Source note | uspto-grants-1989_06 |
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