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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351073Generated: October 30, 2026

Hydroxyamine hydrochloride → HCID 85073502, compound

https://huagongshe.com/reaction/351073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 73989419HCID 73989419—
SolventTetrahydrofuranHCID 8028—
ProductHCID 85073502HCID 8507350230%

Reaction Steps

To a suspension of hydroxylamine hydrochloride (0.21 g, 3.01 mmol) in tetrahydrofuran (4.0 ml) a saturated NaHCO3 solution (2.6 ml) was added and the resultant mixture was stirred at ambient temperature for 25 min. To the reaction mixture a 3-(2-phenylsulfamoyl-phenyl)acryloyl chloride (36a) (0.19 g, 0.59 mmol) solution in tetrahydrofuran (2.5 ml) was added and the mixture was stirred at ambient temperature for 2 hours. The reaction mixture was partitioned between ethyl acetate and 2N HCl. The organic layer was washed successively with water and saturated NaCl, and the solvent was removed. The residue was washed with diethyl ether and crystallised from acetonitrile to give the title compound (0.056 g, 30%) as white crystals, m.p. 205–206.5° C. 1H NMR (DMSO-d6, HMDSO), δ: 6.37 (1H, d, J=16.0 Hz); 6.99–8.04 (10H, m); 8.23 (1H, d, J=116.0 Hz); 10.55 (1H, s); 10.83 (1H, br s). HPLC analysis on Symmetry C18 column: impurities 6.4% (column size 3.9×150 mm; mobile phase acetonitrile—0.1M phosphate buffer, pH 2.5, 30:70; sample concentration 0.2 mg/ml; flow rate 1.2 ml/min; detector UV 220 nm). Anal. Calcd for C15H14N2O4S*0.1H2O, %: C, 56.28; H, 8.75; N, 4.47. Found, %: C, 55.63; H, 9.07; N, 4.36.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183298B2
Source datasetuspto-grants-2007_02
ORD IDord-9a9ecbd89a54400eb7e05f262ea92077
Source noteuspto-grants-2007_02