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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060760Generated: October 25, 2026

Hydroxyamine hydrochloride → 1-[5-Hydroxy-3-(Hydroxymethyl)-2,3-Dihydro-1,4-Benzodioxin-6-yl]-1-Ethanone Oxime

https://huagongshe.com/reaction/1060760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantPyridine ethanolHCID 21975839—
Reactant1-[(3S)-5-hydroxy-3-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxin-6-yl]-1-EthanoneHCID 69017006—
SolventEthanolHCID 702—
Product1-[5-Hydroxy-3-(Hydroxymethyl)-2,3-Dihydro-1,4-Benzodioxin-6-yl]-1-Ethanone OximeHCID 136343266—

Reaction Steps

A solution of hydroxylamine hydrochloride (2.38 g, 34.2 mmole) in 1:1 ethanol/pyridine (100 mL) was added to a solution of 1-[(3S)-5-hydroxy-3-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxin-6-yl]-1-ethanone (1.92 g, 8.57 mmole) in ethanol (200 mL). It was then heated to reflux under nitrogen for 5 hours. Upon cooling, the solvent was removed and replaced with ethyl acetate. The solution was then washed with water (200 mL) and with aqueous 2N HCl (100 mL), dried over magnesium sulfate, filtered and evaporated in vacuum to give 1.89 g (93%) of the (S)-enantiomer of the title compound as a gray solid, m.p. 162° C. MS (ESI) m/z 240 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525075B2
Source datasetuspto-grants-2003_02
ORD IDord-aad265719e22488ba58cb32f6949fc69
Source noteuspto-grants-2003_02