HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Naphthaldehyde → 6-Bromonaphthalene-1-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Naphthaldehyde | HCID 6195 | — |
| Reactant | Bromine | HCID 24408 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 6-Bromonaphthalene-1-carbaldehyde | HCID 13142451 | 36.7% |
Reaction Steps
To a flask fitted with a condenser containing 1-naphthaldehyde (10 g, 64.02 mmol) was added a solution of bromine (3.3 mL, 63.83 mmol) in anhydrous chloroform (15 mL). The reaction mixture was heated under reflux for 3.5, allowed to RT and filtered. The filtrate was washed with water, brine and dried (MgSO4). After evaporation the crude product was purified on silica gel (eluant: hexanes:EtOAc, 98:2) to afford 6-bromo-1-naphthaldehyde 5.5 g (27%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07153875B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-3f81eafd0b224bd48cc62fa725adc873 |
| Source note | uspto-grants-2006_12 |