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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351092Generated: October 30, 2026

Hydroxyamine hydrochloride → HCID 5353765, compound

https://huagongshe.com/reaction/351092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 73989395HCID 73989395—
SolventTetrahydrofuranHCID 8028—
ProductHCID 5353765HCID 5353765—

Reaction Steps

To a suspension of hydroxylamine hydrochloride (0.27 g, 3.88 mmol) in tetrahydrofuran (5 ml) saturated NaHCO3 solution (3 ml) was added and the resultant mixture was stirred at ambient temperature for 10 min. To the reaction mixture a solution of crude 3-[3-(3-methoxy-phenylsulfamoyl)-phenyl]-acryloyl chloride (83a) (0.27 g, 0.68 mmol) in tetrahydrofuran (3.5 ml) was added and the mixture was stirred at ambient temperature for one hour. The reaction mixture was partitioned between ethyl acetate and 2N HCl. The organic layer was washed successively with water and saturated NaCl, then the solvent was removed. The residue was crystallised from acetonitrile and washed with diethyl ether affording the title compound as a white solid (0.1 g, 37%). M.p. 190–191.5° C. 1H NMR (DMSO-d6, HMDSO) δ: 6.29 (1H, d, J=16.0 Hz); 7.16 (2H, d, J=8.0 Hz); 7.24–7.78 (8H, m); 7.86 (4H, m); 8.94 (1H, br s); 10.57 (1H, s); 10.66 (1H, br s). HPLC analysis on Zorbax SB—C18 column: impurities 4% (column size 4.6×150 mm; mobile phase acetonitrile—0.1% H3PO4, gradient from 30 to 100%; sample concentration 0.2 mg/ml; flow rate 1.0 ml/min; detector UV 254 nm). Anal. Calcd for C21H18N2O4S, %: C, 63.94; H, 4.60; N, 7.10. Found, %: C C, 63.64; H, 4.45; N, 7.00.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183298B2
Source datasetuspto-grants-2007_02
ORD IDord-28c8bc9d847a40c9829b682c1c56ed2d
Source noteuspto-grants-2007_02