HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylolpropane → 1-(1-Bromoethyl)-4-ethyl-2,6,7-trioxabicyclo[2.2.2]octane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylolpropane | HCID 6510 | — |
| Reactant | 2-Bromo-1,1,1-triethoxypropane | HCID 2779285 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(1-Bromoethyl)-4-ethyl-2,6,7-trioxabicyclo[2.2.2]octane | HCID 20474833 | 63.7% |
Reaction Conditions
| Temperature | 140 °C |
|---|
Reaction Steps
25.5 g (0.1 moles) of the product obtained in step (a) above, 13.4 g (0.1 moles) of trimethylolpropane and 0.05 g of p-toluenesulfonic acid were placed in a flask fitted with a Dean & Stark condenser and the contents of the flask were heated at 140° C. for about 2 hours. The reaction was stopped when a theoretical amount of ethyl alcohol was evaporated off, after which the reaction solution was distilled under reduced pressure using a Vigreaux distillation column to yield 16 g (63%) of the desired product having a boiling point of 81°-83° C./0.1 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04425473 |
| Source dataset | uspto-grants-1984_01 |
| ORD ID | ord-02791f7f5d8f4b5a8e0a50cffeb017c0 |
| Source note | uspto-grants-1984_01 |