HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973272Generated: October 25, 2026
Sodium hydride → 4-[(Diphenylmethoxy)methyl]-2,2-bis(trifluoromethyl)-1,3-dioxolane
https://huagongshe.com/reaction/1973272
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Bromodiphenylmethane | HCID 236603 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2,2-Bis(trifluoromethyl)-4-hydroxymethyl-1,3-dioxolane | HCID 21997103 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-[(Diphenylmethoxy)methyl]-2,2-bis(trifluoromethyl)-1,3-dioxolane | HCID 21395813 | — |
Reaction Steps
A sample of 12 grams (0.05 mols) of 2,2-bis(trifluoromethyl)-4-hydroxymethyl-1,3-dioxolane in 50 ml toluene is treated with 1.93 grams sodium hydride - mineral oil (53.4%, 0.043 mols) at 25°-33° C. The sodium salt is stirred for 2 hours at 35° C. Benzhydryl bromide, 10.6 grams, (0.043 mols) is added at 37° C. and then the temperature is raised to 75°-95° C. for 3 hours. The mixture is filtered and the filtrate washed with water. Vacuum-stripping gives an oil which is dissolved in methanol and clarified by filtration through Super Cel. Yield of product is 17.0 grams at this point. A forerun is distilled in a 4 inch column filled with stainless steel packing, the remainder without packed column. The product obtained is distilled at 137° C. under 0.45 mm of mercury pressure to yield 2,2-bis(trifluoromethyl)-4-diphenylmethoxymethyl-1,3-dioxolane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03996376 |
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| Source dataset | uspto-grants-1976_12 |
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| ORD ID | ord-baeb09972a6b4fe49cbfcb59191b9a35 |
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| Source note | uspto-grants-1976_12 |
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