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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643661Generated: October 26, 2026

Methylhydroxylamine → HCID 178482037, compound

https://huagongshe.com/reaction/643661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylhydroxylamineHCID 11647—
ReactantSodium ethoxideHCID 2723922—
Reactant(1-(3-Bromophenyl)ethylidene)cyanamideHCID 10966114—
ReactantHCID 178481314HCID 178481314—
SolventEthanolHCID 702—
ProductHCID 178482037HCID 17848203783%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of the HCl salt of methylhydroxylamine (0.19 g, 2.2 mmol, 1 eq) in ethanol (25 mL) at 25° C. was added a 21% solution of NaOEt in ethanol (0.75 mL, 2.0 mmol, 0.9 eq) followed by (1-(3-bromophenyl) ethylidene) cyanamide (0.50 g, 2.2 mmol, 1 eq). After stirring at 25° C. for 10 min, the solvent was removed in vacuo. The residue was redissolved in CH2Cl2 (25 mL), the mixture was filtered, and the solvent was removed in vacuo to give 0.5 g (83%) of 5-(3-bromophenyl)-2,5-dimethyl-1,2,4-oxadiazolidin-3-imine (DB2, R1=Me, R4=Me) as a colorless oil: 1H NMR (CDCl3) δ 7.63 (t, J=1.8 Hz, 1H), 7.52. (dd, J=2.0, 1.1 Hz, 1H), 7.38 (dd, J=2.0, 1.1 Hz, 1H), 7.29 (t, J=7.9 Hz, 1H), 3.28 (s, 3H), 1.88 (s, 3H). MS (ESI) m/e 270.0, 272.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700603B2
Source datasetuspto-grants-2010_04
ORD IDord-b31cedebed924a7da6632adce1fcf9ca
Source noteuspto-grants-2010_04