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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119322Generated: October 31, 2026

Hydrochloric Acid → HCID 10277798, compound

https://huagongshe.com/reaction/2119322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantOxalyl chlorideHCID 65578—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 10276904HCID 10276904—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 10277798HCID 1027779890.3%

Reaction Steps

The carboxylic acid obtained in Example 1 (12.2 g, 0.026 mol) was diluted with dichloromethane (150 mL) and oxalyl chloride (16.5 g, 0.13 mol). N,N-Dimethylformamide was added as a catalyst. The solution was stirred at room temperature for 14 hours, at which time the solvent was concentrated in vacuo. The crude acid chloride was triturated with hexane and collected by filtration. The solid was diluted with tetrahydrofuran (75 mL) and added dropwise to a mixture of hydroxylamine hydrochloride (9 g, 0.13 mol) and sodium bicarbonate (16.4 g, 0.19 mol) in tetrahydrofuran (150 mL)/water (75 mL) cooled to 0° C. The reaction mixture gradually warmed to room temperature and was stirred for 14 hours. Ethyl acetate and aq. HCl (1M) were added, the layers were separated, and the organic portion was washed with brine, dried (MgSO4), and concentrated. The resulting viscous liquid yielded a white solid (11.4 g, 90%) upon treatment with cold diethyl ether/petroleum ether (4:1), mp 190-192° C.; 1HNMR (DMSO-d6) δ 10.7 (s, 1H), 8.9 (s, 1H), 4.1 (s, 1H), 4.0 (m, 1H), 3.8 (m, 1H), 2.9 (m, 1H), 2.5 (m, 1H), 1.4, (s, 3H), 1.1 (s, 3H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06686355B2
Source datasetuspto-grants-2004_02
ORD IDord-3d14557ebaee41e2944843cc406bbb1c
Source noteuspto-grants-2004_02