HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976998Generated: November 1, 2026
Glycerol → 2,2-Bis(trifluoromethyl)-4-hydroxymethyl-1,3-dioxolane
https://huagongshe.com/reaction/1976998
Participants
| Role | Name | HCID | Charge |
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| Reactant | Glycerol | HCID 753 | — |
| Reactant | Hexafluoroacetone | HCID 12695 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2,2-Bis(trifluoromethyl)-4-hydroxymethyl-1,3-dioxolane | HCID 21997103 | — |
Reaction Steps
In a 4 L round bottom flask, hexafluoroacetone (99.7 g; 0.6 moles) was condensed at 0° C. into a well stirred solution of glycerol (55.3 g; 0.6 moles) in 500 mL of anhydrous ethylene glycol dimethyl ether. After the addition of hexafluoroacetone was complete, the solution was allowed to warmn to ambient temperature. Next, a solution of 1,3-dieyclohexylcarbodiimide (136.2 g; 0.66 moles) in 2 L of anhydrous ethylene glycol dimethyl ether was added slowly to the resulting hemiketal solution over a period of about one and a half hours. The combined solution was stirred for an additional hour and then the low boiling solvent was removed using a rotary evaporator. The remaining liquid was transferred to a 250 mL round bottom flask and the liquid heated with stirring at 100° C. for 1 hour. While continuing to heat the liquid, the product was isolated by vacuum distillation at 76° C. and 18 mm of Hg. The yield of product was 117 g which is 81% of the theoretical value.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06231655B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-da05c9d2837d40899a03fa36070770e3 |
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| Source note | uspto-grants-2001_05 |
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