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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846885Generated: October 30, 2026

Sodium Carbonate → HCID 19022411, compound

https://huagongshe.com/reaction/846885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantBromineHCID 24408—
ReactantSodium SulfiteHCID 24437—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 19022416HCID 19022416—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 19022411HCID 19022411—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution, cooled to 0° C., of 16.5 g of 2,2-di-methyl-5-(methylsulphinyl)-1,3-benzodioxol and 6.2 g of pyridine in 230 ml of methylene chloride, there were added in succession 5.43 g of bromine and 12.1 g of N-bromosuccin-imide. The reaction mixture was stirred at 0° C. for 3 hours and then at 20° C. for a further 12 hours. The orange colored solution was cooled to 0° C., treated with 40 ml of 1M aqueous sodium sulphite solution and the pH of the mixture was adjusted to 7 by the addition of 17% aqueous sodium carbonate solution. After stirring for 10 minutes, the phases were separated. The organic phase was washed in succession with 50 ml of 1N aqueous hydrochloric acid, 50 ml of 5% sodium hydrogen carbonate solution and 3 times with 100 ml of water each time, dried over sodium sulphate and evaporated in a vacuum. The residue was chromatographed on silica gel, with elution being carried out with ethyl acetate/hexane (1:2, v/v). After crystallization from acetone/water, there was obtained 5-[(bromomethyl)-sulphinyl]-1,3-benzodioxol as white crystals having a melting point of 88°-89° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05138066
Source datasetuspto-grants-1992_08
ORD IDord-cf34d0d49c574bff973a07501e87f36e
Source noteuspto-grants-1992_08