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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351083Generated: October 30, 2026

Dichloromethane → HCID 9902605, compound

https://huagongshe.com/reaction/351083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium BicarbonateHCID 516892—
Reactant(E)-5-(3-Phenylsulfamoylphenyl)pent-2-en-4-ynoic acidHCID 22492410—
SolventWaterHCID 962—
ProductHCID 9902605HCID 9902605—

Reaction Steps

To a solution of (E)-5-(3-phenylsulfamoylphenyl)pent-2-en-4-ynoic acid (56a) (0.25 g 0.77 mmol) in methylene chloride (5 ml) oxalyl chloride (0.42 g 3.1 mmol) was added. The resultant mixture was stirred for 1 hour at ambient temperature and the solvents were removed under reduced pressure. The crude product (57a) was dissolved in acetonitrile (5 ml) and the obtained solution to a mixture of hydroxylamine hydrochloride (0.3 g, 4.3 mmol) and NaHCO3 (0.3 g, 3.6 mmol) in water (8 ml) was added. The reaction mixture was stirred for 10 min. and the product was extracted with ethyl acetate (30 ml). The extract was washed with 10% Na2CO3, and the aqueous phase was acidified with 3% HCl. The precipitate was filtered and dried to give the title compound (0.12 g, (46%). M.p 88–90° C. 1H NMR (DMSO-d6, HMDSO) δ: 6.41 (1H, d, J=115.8 Hz, CH); 6.82 (1H, d, J=15.8 Hz, CH); 6.92–7.41 (5H, m, C6H5); 7.47–8.01 (4H, m, C6H4); 8.94–11.21 (3H, br s, NH, NH, OH). Anal. Calcd for C17H14N2O4S*0.4H2O: C, 58.58; H, 4.27; N, 8.01. Found: C, 58.12; H, 4.03; N, 7.80.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183298B2
Source datasetuspto-grants-2007_02
ORD IDord-9a05388ecf1d4853a18eeb88add50c8b
Source noteuspto-grants-2007_02