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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769962Generated: October 25, 2026

Hydrochloric Acid → 3-[Benzo-1,2,3-thiadiazol-7-yl]acrylic acid

https://huagongshe.com/reaction/1769962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMalonic AcidHCID 867—
ReactantPyridineHCID 1049—
ReactantBenzo[d][1,2,3]thiadiazole-7-carbaldehydeHCID 14835681—
SolventSodium HydroxideHCID 14798—
Product3-[Benzo-1,2,3-thiadiazol-7-yl]acrylic acidHCID 54496090447.6%

Reaction Steps

A mixture of 1.96 g of benzo-1,2,3-thiadiazole-7-carbaldehyde, 1.24 g of malonic acid and 6 ml of pyridine are heated for 26 hours at 120° C., with 2 further additions of 0.6 g portions of malonic acid after 4 and 7 hours. The mixture is then cooled, poured into ice-water and acidified with concentrated hydrochloric acid. The precipitate which has formed is faltered off and dissolved in dilute sodium hydroxide solution, the mixture is washed three times with methylene chloride, and the aqueous phase is subsequently acidified once more, using hydrochloric acid. The precipitate obtained is filtered off, washed with water and dried in vacuo, resulting in 11 g of the title compound of m.p. 199°-202° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05384321
Source datasetuspto-grants-1995_01
ORD IDord-4ee0d24133594dcb8030147d7c8e9ff5
Source noteuspto-grants-1995_01