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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386418Generated: November 1, 2026

(Aminooxy)acetic acid → HCID 54363749, compound

https://huagongshe.com/reaction/1386418

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Aminooxy)acetic acidHCID 286—
ReactantHydrochloric AcidHCID 313—
Reactant6-(2-Imidazole-1-yl-ethoxy)-3,4-dihydro-2H-naphthalen-1-oneHCID 15486912—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductHCID 54363749HCID 5436374943.6%

Reaction Steps

A solution of 1.0 g (3.9 mmol) of 6-[2-(1H-1-imidazolyl)ethoxy]-1,2,3,4-tetrahydro-1-naphthalenone in 10 mL of pyridine was treated with 1.02 g (9.3 mmol) of carboxymethoxyamine×0.5 HCl and the solution heated at reflux for 2 days. The solution was diluted with H2O and extracted with EtOAc. On standing, the aqueous phase deposited a solid which was collected and dried. There was obtained 0.56 g (43% yield) of the product as a white solid, mp 193-195° C. The structure was confirmed by NMR and mass spectroscopy. MS m/z 330 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265422B1
Source datasetuspto-grants-2001_07
ORD IDord-e2f3ea0138f646ad959672103d956c89
Source noteuspto-grants-2001_07