HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Methylhydroxylamine hydrochloride → 5-tert-butyl-1-indanone O-methyloxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | 5-Tert-butyl-2,3-dihydroinden-1-one | HCID 11030576 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 5-tert-butyl-1-indanone O-methyloxime | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08026256B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-21d60427599a4c2cb94d0b704c1d126c |
| Source note | uspto-grants-2011_09 |