HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylolpropane → 2,6,7-Trioxabicyclo(2.2.2)octane, 4-ethyl-1-methyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylolpropane | HCID 6510 | — |
| Reactant | 2-Methylbenzenesulfonic acid | HCID 6925 | — |
| Reactant | Triethyl orthoacetate | HCID 66221 | — |
| Product | 2,6,7-Trioxabicyclo(2.2.2)octane, 4-ethyl-1-methyl- | HCID 165205 | — |
Reaction Steps
Trimethylolpropane (268.0 g, 2.0 mol), triethyl orthoacetate (356.4 g, 2.20 mol) and toluene sulfonic acid (4.0 g) were charged into a oven dried round bottom flask equipped with a stirring bar, distillation head and under nitrogen. The resulting solution was heated until the theoretical amount od ethanol was collected. The reaction was cooled to room temperature. Fractional vacuum distillation afforded the product as a water clear liquid, boiling point 62.8-71.2° C. at 0.78-1.80 torr. Yield: 276.0 g (87.3%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07888440B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-affc0aa3faf54018902545206ae53976 |
| Source note | uspto-grants-2011_02 |