HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 3-bromoquinoline 1-oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Peracetic Acid | HCID 6585 | — |
| Reactant | 3-Bromoquinoline | HCID 21413 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-bromoquinoline 1-oxide | HCID 818076 | 100.9% |
Reaction Steps
To a solution of 3-Bromoquinoline 5 (2.08 g, 10 mmol) in CHCl3 (5 ml) was added CH3CO2OH (5 ml, 32% solution in dilute HOAc, 20 mmol) and the mixture was stirred overnight. Acetone (3 ml) was added and the mixture was stirred an additional 15 min then poured into saturated NaHCO3 (aq) and extracted with CH2Cl2. The combined extracts were dried (K2CO3) and concentrated to yield pure 6 (2.26 g, 100%) as a tan solid. 1H NMR d (d=delta) (ppm): 7.7 dd (CH atom), 7.8 m (2 CH atom), 7.9 s (CH atom), 8.6 s (CH atom), 8.7 d (CH atom).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05372813 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-d050b458a34e451b9cf159387ad35a4e |
| Source note | uspto-grants-1994_12 |