HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 5-Bromo-2-isopropylbenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2-(Propan-2-yl)benzaldehyde | HCID 590536 | — |
| Reactant | N-Bromosuccinamide | HCID 9834204 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 5-Bromo-2-isopropylbenzaldehyde | HCID 58340835 | 58.7% |
Reaction Steps
To a solution of trifluoroacetic acid (50 ml) and 2-isopropylbenzaldehyde (2.0 g, 13.5 mmol) was added conc. sulphuric acid (98%) (10 ml) at room temperature, followed by N-bromosuccinamide (NBS, 3.6 g 20.2 mmol) in portions. After 2 hrs, the mixture was poured into ice water and extracted with dichloromethane (3×30 mL). The organic layers were combined and neutralized with saturated aqueous sodium bicarbonate, washed with brine (30 mL), dried over sodium sulfate and concentrated. The resulting residue was purified by column chromatography to furnish 5-bromo-2-isopropylbenzaldehyde (1.80 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08828951B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-ee557a7feafe40a1af75b03740360b77 |
| Source note | uspto-grants-2014_09 |