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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2350984Generated: November 1, 2026

Dibromomethane → HCID 13592052, compound

https://huagongshe.com/reaction/2350984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibromomethaneHCID 3024—
ReactantEthyl vinyl etherHCID 8023—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Hydroxy-4,6,7-trimethyl-2H-1,3-benzoxathiol-2-oneHCID 13089352—
CatalystMethanesulfonic AcidHCID 6395—
CatalystTrioctylmethylammonium chlorideHCID 21218—
SolventWaterHCID 962—
ProductHCID 13592052HCID 13592052—

Reaction Conditions

Temperature-20 °C

Reaction Steps

A mixture of 7.35 g of 5-hydroxy-4,6,7-trimethyl-1,3-benzoxathiole-2-one, 20 ml of ethyl vinyl ether and 20 ml of methylene dibromide was cooled down to -20° C. under a stream of nitrogen, and then 20 mg of methanesulfonic acid were added dropwise, while stirring. After completion of the dropwise addition, the reaction temperature was gradually raised to room temperature, and the mixture was stirred for 3 hours at room temperature. To this reaction mixture were added 30 ml of water, 8.8 g of sodium bicarbonate and 1.0 g of Aliquat 336 (a trade mark for methyltrioctylammonium chloride), and the mixture was heated under reflux for 9 hours, which caused the excess methylene dibromide to vaporize gradually and leave a crude oil. This crude oil was extracted with diethyl ether, and the extract was dried over anhydrous sodium sulfate. The ether was then distilled off, to yield 12 g of an oily substance, which was purified by silica gel column chromatography. From the portion which could be eluted with a 20:1 by volume mixture of petroleum ether and diethyl ether were obtained 5.2 g of the title compound melting at 52°-54° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04871762
Source datasetuspto-grants-1989_10
ORD IDord-86c1e0c8a26649409d734d56d50211ed
Source noteuspto-grants-1989_10