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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantWaterHCID 962—
Reactant6-Bromo-5-methyl-2,3-dihydro-1,4-benzodioxineHCID 12464527—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product5-Methyl-2,3-dihydro-1,4-benzodioxine-6-carboxylic acidHCID 1070295977%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05378726
Source datasetuspto-grants-1995_01
ORD IDord-d078251872f448e7b8f5d22637e8a05c
Source noteuspto-grants-1995_01