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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900866Generated: October 26, 2026

Serinol → 5-Chloro-4-nitro-thiophene-2-sulfonic acid (2-hydroxy-1-hydroxymethyl-ethyl)-amide

https://huagongshe.com/reaction/900866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSerinolHCID 68294—
Reactant5-Chloro-4-nitrothiophene-2-sulfonyl chlorideHCID 2735783—
ReactantMagnesium monoxideHCID 6850729—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-4-nitro-thiophene-2-sulfonic acid (2-hydroxy-1-hydroxymethyl-ethyl)-amideHCID 6721871244%

Reaction Steps

To a stirred solution of 2-amino-1,3-propanediol (0.5 g, 5.49 mmol) in water (2 ml) was added at room temperature magnesium oxide (1.11 g, 27.5 mmol) and THF (6 ml). The suspension was stirred at room temperature for 30 min and a solution of 5-chloro-4-nitrothiophene-2-sulfonyl chloride (2.88 g, 10.9 mmol) in THF (2 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 column chromatography on silica gel (heptane/ethyl acetate 1:1) and subsequent crystallization from ethyl acetate/hexane to yield 5-chloro-4-nitro-thiophene-2-sulfonic acid (2-hydroxy-1-hydroxymethyl-ethyl)-amide (0.76 g, 44%) as a light yellow solid. MS (ISP) 314.9 [(M−H)−], mp 142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361659B2
Source datasetuspto-grants-2008_04
ORD IDord-cc7f0ce942904c4f964f21d8a02faea9
Source noteuspto-grants-2008_04