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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223382Generated: November 1, 2026

O-Methylhydroxylamine hydrochloride → 5-tert-butyl-1-indanone O-methyloxime

https://huagongshe.com/reaction/2223382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
Reactant5-Tert-butyl-2,3-dihydroinden-1-oneHCID 11030576—
SolventPyridineHCID 1049—
Product5-tert-butyl-1-indanone O-methyloximeHCID 73047460—

Reaction Steps

5-tert-Butyl-1-indanone (13.41 g, 71.23 mmol) and methoxyamine hydrochloride (6.68 g, 80 mmol) were disolved in pyridine (75 ml) and stirred at ambient temperature for 16 hours. The mixture was evaporated under reduced pressure and the residue was partitioned between water and diethyl ether (×2). The combined organic layers were washed with 1N aqueous hydrochloric acid, dried with magnesium sulfate, and the filtrate was evaporated under reduced pressure to provide the title compound which was used without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375126B2
Source datasetuspto-grants-2008_05
ORD IDord-7a8ca06823754499b44f77b92a3416da
Source noteuspto-grants-2008_05