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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258704Generated: October 30, 2026

HCID 53940535, compound → HCID 21426445, compound

https://huagongshe.com/reaction/258704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 53940535HCID 53940535—
SolventSulfuric AcidHCID 1118—
ProductHCID 21426445HCID 2142644560.2%

Reaction Steps

Ethyl (2-methylthio-imidazol-1-yl)-acetate (14.5 g.) in 4 N sulphuric acid (30 cc.) is heated under reflux for 1 hour. The sulphate ions are then removed by adding an aqueous solution of barium hydroxide and filtering off the precipitated barium sulphate. The filtrate is treated with decolorising charcoal and is then concentrated to dryness under reduced pressure (20 mm.Hg). The residue is taken up in benzene (80 cc.) and the mixture is again concentrated to dryness under reduced pressure (20 mm.Hg); this step is then repeated. Purification of the product by recrystallisation from dimethylformamide (30 cc.) yields (2-methylthio-imidazol-1-yl)-acetic acid (7.5 g.), m.p. 176° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04034088
Source datasetuspto-grants-1977_07
ORD IDord-35f125855483496fa6611390265065df
Source noteuspto-grants-1977_07