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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912629Generated: October 25, 2026

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

https://huagongshe.com/reaction/912629

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 (X2). 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 numberUS08026256B2
Source datasetuspto-grants-2011_09
ORD IDord-21d60427599a4c2cb94d0b704c1d126c
Source noteuspto-grants-2011_09