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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197700Generated: November 1, 2026

Sulfuric Acid → HCID 19107715, compound

https://huagongshe.com/reaction/1197700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
Reactant3-Bromo-2-methylpropionic acidHCID 304776—
ReactantPotassium thiocyanateHCID 516872—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 19107715HCID 19107715—

Reaction Conditions

Temperature0 °C

Reaction Steps

16.7 g of 2-methyl-3-bromopropionic acid are dissolved in 50 ml of toluene, the solution obtained is cooled to 0° C., then 19.42 g of potassium rhodanide and 5 ml of water are added. The pH value of the reaction mixture is adjusted to 6.5 by the dropwise addition of 10 n sodium hydroxide. The pale yellow biphasic solution obtained is stirred at 25° C. for 48 hours while maintaining the pH value between 6.4 and 6.6 by adding further amounts of sodium hydroxide as required. The reaction mixture is cooled to 0° C. and adjusted to a pH value of 2.7 by adding 10 n sulfuric acid, then filtered and the organic phase is separated. The aqueous phase is extracted 5 times with 20 ml of toluene, the organic solutions are combined and extracted with 10 ml of water. The pale yellow toluene solution is dried over anhydrous magnesium sulfate and evaporated under reduced pressure to obtain 11.13 g /76.7%/ of 2-methyl-3-thiocyanatopropionic acid, m.p.: 24°-25° C. Based on determination by gas chromatography, the purity of the product is 98 to 99 per cent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05276207
Source datasetuspto-grants-1994_01
ORD IDord-5c24d1f815684bf585c47c0ff95e51c7
Source noteuspto-grants-1994_01