HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358071Generated: October 26, 2026
Ethanol → (1-Methyl-2,6,7-trioxabicyclo[2.2.2]octan-4-yl)methanol
https://huagongshe.com/reaction/1358071
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Pentaerythritol | HCID 8285 | — |
| Reactant | Triethyl orthoacetate | HCID 66221 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | (1-Methyl-2,6,7-trioxabicyclo[2.2.2]octan-4-yl)methanol | HCID 13547990 | 88.8% |
Reaction Steps
Into a flask equipped with a stirrer, a distilling column, a nitrogen inlet, a heating jacket, and a thermometer were charged 486 g of triethyl orthoacetate, 408 g of pentaerythritol, 300 g of diethylene glycol dimethyl ether, and 0.9 g of PTSA. The mixture was gradually heated to 170° C. over a period of 5 hours. During this time 490 g of distillate were obtained. The distillate contained mostly ethanol and small amounts of diethylene glycol dimethyl ether. The temperature was lowered to 100° C., and the remaining diethylene glycol dimethyl ether was distilled off under reduced pressure (30 mbar). The residue was subjected to vacuum distillation. The fraction having a boiling temperature of 126-130° C. at a pressure of 4 mbar yielded 426 g of oil. This oil solidified to a clear solid having a melting point of 99° C. and had the following structure
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06593479B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-97c0cfc3ce434984a1ca05f54715e7a7 |
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| Source note | uspto-grants-2003_07 |
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