HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739050Generated: October 27, 2026
1,1-Dibromoethane → 5,8-Dimethyl-1,3-benzodioxane
https://huagongshe.com/reaction/1739050
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1-Dibromoethane | HCID 11201 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,6-Dimethylbenzene-1,2-diol | HCID 11469114 | — |
| Reactant | 5,8-Dimethyl-2,3-dihydro-1,4-benzodioxine | HCID 13067773 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 5,8-Dimethyl-1,3-benzodioxane | HCID 21840481 | — |
Reaction Steps
5,8-Dimethyl-1,4-benzodioxane. To a stirred solution of 3 g of 3,6-dimethylcatechol and 6.15 g of potassium carbonate in 35 mL of ethylene glycol is added 3.74 mL of dibromoethane. A reflux condenser is attached and the mixture heated in an oil bath to 120° C. for 4 hours. The mixture is allowed to cool to room temperature and then is distributed between 100 mL of saturated potassium carbonate solution and 200 mL of ether. The ether layer is dried over magnesium sulfate and concentrated under reduced pressure to yield a red liquid, which is purified by chromatography on silica gel to afford 2.90 g of 5,8-dimethyl-1,3-benzodioxane as a light yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05965595 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-598fb41a9e004acfa6ed3d8b9d9d91bd |
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| Source note | uspto-grants-1999_10 |
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