HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241503Generated: October 30, 2026
Pyridine → 7-chloro-3,4-dihydro-2H-naphthalen-1-one-O-methyl-oxime
https://huagongshe.com/reaction/241503
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 7-Chloro-1,2,3,4-tetrahydronaphthalen-1-one | HCID 256677 | — |
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 7-chloro-3,4-dihydro-2H-naphthalen-1-one-O-methyl-oxime | HCID 86699876 | 100% |
Reaction Steps
To a stirred solution of 7-chloro-1-tetralone CAS: 26673-32-5 (5.0 g; 27.68 mmol) in methanol (55 ml) was added pyridine (2.87 ml; 34.05 mmol) followed by a portion wise addition of methoxyamine hydrochloride (2.84 g; 34.05 mmol). The reaction mixture was stirred at 24° C. for 16 h under nitrogen. Methanol was removed under reduced pressure, the residue poured in water (300 ml) and 1N hydrochloric acid was added (100 ml). The solution was extracted with dichloromethane (3×150 ml). Combined organic layers were washed with water (300 ml) and dried over sodium sulfate. The solvent was removed in vacuo to afford 6.22 g (100% of theory) of crude 7-chloro-3,4-dihydro-2H-naphthalen-1-one-O-methyl-oxime as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08653003B2 |
|---|
| Source dataset | uspto-grants-2014_02 |
|---|
| ORD ID | ord-d23521188cca4cfaab81244a486e6095 |
|---|
| Source note | uspto-grants-2014_02 |
|---|