HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351092Generated: October 30, 2026
Hydroxyamine hydrochloride → HCID 5353765, compound
https://huagongshe.com/reaction/351092
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 73989395 | HCID 73989395 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 5353765 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07183298B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-28c8bc9d847a40c9829b682c1c56ed2d |
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| Source note | uspto-grants-2007_02 |
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