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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900868Generated: October 31, 2026

Ethanolamine → HCID 67219177, compound

https://huagongshe.com/reaction/900868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
Reactant5-Chloro-4-nitrothiophene-2-sulfonyl chlorideHCID 2735783—
ReactantMagnesium monoxideHCID 6850729—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67219177HCID 6721917744.1%

Reaction Steps

To a stirred solution of ethanolamine (0.67 g, 11 mmol) in water (4 ml) was added at room temperature magnesium oxide (2.22 g, 55 mmol) and THF (12 ml). The suspension was stirred at room temperature for 30 min and a solution of 5-chloro-4-nitrothiophene-2-sulfonyl chloride (3.46 g, 13.2 mmol) in THF (4 ml) was added. The light yellow suspension was stirred at room temperature for 1 h and, after filtration on Dicalit, evaporated. Water (60 ml) was added and the mixture was extracted with ethyl acetate (3×50 ml). The combined organic layers were washed with brine (70 ml), dried (MgSO4) and evaporated. The crude product was further purified by flash chromatography on silica gel (heptane/ethyl acetate) and subsequent crystallization from ethyl acetate/hexane to yield 5-chloro-4-nitro-thiophene-2-sulfonic acid (2-hydroxy-ethyl)-amide (1.39 g, 44%) as a yellow solid. MS (ISP) 284.8 [(M−H)−], mp 99° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361659B2
Source datasetuspto-grants-2008_04
ORD IDord-b043b2ad3ab645b89a190161c141f5b3
Source noteuspto-grants-2008_04