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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258869Generated: October 31, 2026

Trifluoroacetic acid → 5-Bromo-2-isopropylbenzaldehyde

https://huagongshe.com/reaction/1258869

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 numberUS08466114B2
Source datasetuspto-grants-2013_06
ORD IDord-e448c0a2908449b2ac104c5dbe6f6b22
Source noteuspto-grants-2013_06