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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016087Generated: October 31, 2026

Triethylamine → HCID 18758447, compound

https://huagongshe.com/reaction/1016087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantGlyoxylic acid, monohydrateHCID 15620607—
ReactantEthyl 3-[(1,3-benzothiazol-2-yl)sulfanyl]-2-oxopropanoateHCID 67300216—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 18758447HCID 18758447—

Reaction Steps

To a solution of glyoxylic acid monohydrate (98 mg, 1.03 mmol) in 6 mL methylenechloride/methanol (5:1) was added triethylamine (418 μL, 3.0 mmol) and stirred vigorously. 3-(benzothiazol-2-ylsulfanyl)-2-oxo-propionic acid ethyl ester (281 mg, 1.06 mmol) in 6 mL methylenechloride/methanol (5:1) was added dropwise over a period of 3 hours and the reaction was stirred overnight (15 hrs) at room temperature. The reaction mixture was then neutralized with NaH2PO4 and washed with ethylacetate. The resulting very polar product remained in the aqueous layer and was purified by reverse-phase HPLC. The pure fractions were pooled and concentrated under reduced pressure. Upon evaporation of solvent, 3-(benzothiazol-2-ylsulfanyl)-4-hydroxy-5-oxo-2,5-dihydro-furan-2-carboxylic acid precipitated out (70 mg) as a white solid which was filtered and washed with water. The filtrate was collected and lyophilized to afford a pale yellow solid which was determined to be the triethylamine salt of the desired product. 1H-NMR (MeOD, 300 MHz) δ (ppm): 7.92-7.87 (m, 2H), 7.51-7.38 (m, 2H), 5.68 (s, 1H). MS (ESI) m/z: 310 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985771B2
Source datasetuspto-grants-2011_07
ORD IDord-d1bbf53feeab4ee3b761e376e285229a
Source noteuspto-grants-2011_07