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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111358Generated: October 29, 2026

Oxalic Acid → HCID 3076377, compound

https://huagongshe.com/reaction/1111358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalic AcidHCID 971—
ReactantSodium HydroxideHCID 14798—
ReactantBromineHCID 24408—
ReactantPotassium thiocyanateHCID 516872—
ReactantHCID 14836843HCID 14836843—
SolventAcetic AcidHCID 176—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 3076377HCID 3076377146.9%

Reaction Steps

Bromine (3.2 g; 1 cc) is added at room temperature to 3-(4-trifluoromethoxyanilino)propionitrile (3 g) and potassium thiocyanate (7.8 g) dissolved in acetic acid (50 cc). Stirring is maintained for 12 hours at this temperature. The mixture is evaporated to dryness at 80° C. under reduced pressure (20 mm Hg; 2.7 kPa). The residue obtained is taken up with water (100 cc) and the pH is brought to 9-10 by adding concentrated sodium hydroxide (10N). After extraction with ethyl acetate (2×50 cc, washing of the combined phases with water (2×20 cc), drying over anhydrous magnesium sulphate and evaporation to dryness at 40° C. under reduced pressure (20 mm Hg; 2.7 kPa), a brown oil is isolated. This oil is dissolved in acetone (100 cc) and oxalic acid (2 g) is added. 2-Imino-3-(2-cyanoethyl)-6-trifluoromethoxy-benzothiazoline (5.5 g) is thereby isolated in the form of a monooxylate, m.p. 180° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04980356
Source datasetuspto-grants-1990_12
ORD IDord-1b353a6291eb49c9be7fc277af7b6380
Source noteuspto-grants-1990_12