HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-(Bromomethyl)-2,6,7-trioxabicyclo[2.2.2]octane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | HCID 14646171 | HCID 14646171 | — |
| Product | 4-(Bromomethyl)-2,6,7-trioxabicyclo[2.2.2]octane | HCID 20274483 | — |
Reaction Steps
Monobromopentaerythritol from A (10 g, 0.05 mole) and 9 ml triethylorthoformate (0.05 mole) are mixed in a sublimation apparatus equipped with a side arm. The mixture is heated to about 100° C. with magnetic stirring, and 1,5 equivalents of ethanol are allowed to distill out. Then about 100 ml dioctyl phthalate and a trace of anhydrous p-toluenesulfonic acid are added. Under vacuum the mixture is heated to about 140°-150° C. Periodically the collected crystals are removed from the cold finger. After about 3 hours no more compound sublimes. The yield of 4-bromoethyl-2,6,7-trioxabicyclo[2.2.2]octane is 6.5 g (60%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04405798 |
| Source dataset | uspto-grants-1983_09 |
| ORD ID | ord-6b13e76a6ed34c6db0bb8e55d028fe34 |
| Source note | uspto-grants-1983_09 |