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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295527Generated: November 1, 2026

Trimethylolpropane → 1-(1-Bromoethyl)-4-ethyl-2,6,7-trioxabicyclo[2.2.2]octane

https://huagongshe.com/reaction/2295527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylolpropaneHCID 6510—
Reactant2-Bromo-1,1,1-triethoxypropaneHCID 2779285—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventEthanolHCID 702—
Product1-(1-Bromoethyl)-4-ethyl-2,6,7-trioxabicyclo[2.2.2]octaneHCID 2047483363.7%

Reaction Conditions

Temperature140 °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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04425473
Source datasetuspto-grants-1984_01
ORD IDord-02791f7f5d8f4b5a8e0a50cffeb017c0
Source noteuspto-grants-1984_01