HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768665Generated: October 27, 2026
Carbon Dioxide → 5-Methyl-2,3-dihydro-1,4-benzodioxine-6-carboxylic acid
https://huagongshe.com/reaction/1768665
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 6-Bromo-5-methyl-2,3-dihydro-1,4-benzodioxine | HCID 12464527 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Methyl-2,3-dihydro-1,4-benzodioxine-6-carboxylic acid | HCID 10702959 | 77% |
Reaction Steps
In 300 ml of dry tetrahydrofuran, was dissolved 32.0 g of 6-bromo-5-methyl-1,4-benzodioxane and after cooling the solution to -78° C., 96.7 ml of n-butyl lithium (n-hexane solution) was added dropwise over 20 minutes or more. After stirring at the same temperature for 1.5 hours, the reaction mixture was poured onto crushed dry ice and dry ice was sublimated while stirring. Water was added to the mixture and the tetrahydrofuran was removed under reduced pressure. The resulting alkaline aqueous solution was washed with methylene chloride and adjusted to pH 3 with a 5% hydrochloric acid, and the precipitated crystals were collected by filtration and dried to obtain 20.9 g of 5-methyl-1, 4-benzodioxan-6-carboxylic acid (yield: 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05378726 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-d078251872f448e7b8f5d22637e8a05c |
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| Source note | uspto-grants-1995_01 |
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