HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromo-1-indanone → 1H-Inden-1-one, 5-bromo-2,3-dihydro-, O-methyloxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromo-1-indanone | HCID 520695 | — |
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 1H-Inden-1-one, 5-bromo-2,3-dihydro-, O-methyloxime | HCID 73012840 | — |
Reaction Steps
5-Bromo-1-indanone and O-methylhydroxylamine hydrochloride were combined in pyridine and stirred at ambient temperature for 16 hours. The mixture was concentrated under reduced pressure and the residue was suspended in diethyl ether. The suspension was filtered and the filter cake was washed with diethyl ether. The filtrate was washed with water, 1N HCl, water, and concentrated to provide the title compound. 1H NMR (300 MHz, d6-DMSO) 7.63 (m, 2H), 7.48 (m, 2H), 3.90 (s, 3H), 3.00 (m, 2H), 2.80 (m, 2H); MS (DCI/NH3) m/e 240 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08487116B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-42ba72b6a0a04af491644634960997b6 |
| Source note | uspto-grants-2013_07 |