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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695875Generated: November 1, 2026

Trifluoroacetic acid → 5-Bromo-2-isopropylbenzaldehyde

https://huagongshe.com/reaction/1695875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-(Propan-2-yl)benzaldehydeHCID 590536—
ReactantN-BromosuccinamideHCID 9834204—
SolventSulfuric AcidHCID 1118—
Product5-Bromo-2-isopropylbenzaldehydeHCID 5834083558.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163704B2
Source datasetuspto-grants-2012_04
ORD IDord-8905e9ffb1e943dbb711267599e2bc40
Source noteuspto-grants-2012_04