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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096707Generated: November 1, 2026

Hydroxyamine hydrochloride → HCID 66781584, compound

https://huagongshe.com/reaction/1096707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium AcetateHCID 517045—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 59779113HCID 59779113—
CatalystNickel DichlorideHCID 24385—
SolventMethanolHCID 887—
ProductHCID 66781584HCID 66781584—

Reaction Steps

To a solution of 5-p-tolyl-bicyclo[3.1.0]hexan-2-one (100 mg, 0.54 mmol) and anhydrous NaOAc (87.5 mg, 1.1 mmol) in anhydrous MeOH (10 mL) was added with stirring NH2OH.HCl (69.5 mg, 1 mmol). The resulting mixture was stirred at room temperature for 18 h. The reaction mixture was filtered and the filtrate was concentrated in vacuo. The residue, dioxime [IS THIS CORRECT?] was reconstituted in anhydrous MeOH (5 ml) and anhydrous NiCl2 (194 mg, 1.5 mmol) was added with stirring. The reaction mixture was cooled to −30° C. and NaBH4 (567 mg, 15 mmol) was added in small portions. After completion of the addition the mixture was allowed to warm to room temperature and concentrated in vacuo. This was then basified with aqueous solution of NaOH and extracted with CH2Cl2 (3×). Organic phases were concentrated and purified by silica gel chromatography. The oily product was converted to HCl salt (62 mg, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138377B2
Source datasetuspto-grants-2012_03
ORD IDord-8c5edd60ef5c465083659a9d2930d129
Source noteuspto-grants-2012_03