Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438406Generated: November 3, 2026

2-Bromo-4-tert-butylbenzaldehyde → HCID 20382954, compound

https://huagongshe.com/reaction/1438406

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-4-tert-butylbenzaldehydeHCID 29923446—
ReactantButyllithiumHCID 178418339—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20382954HCID 2038295481.4%

Reaction Steps

To a stirred suspension of methyltriphenylphosphonium bromide (12.3 g, 33.7 mmol) in anhydrous THF (40 ml) was added n-butyl lithium (1.60 mol/l, hexane solution) (33.7 mmol, 21.1 ml) at 0° C. After 30 minutes at 0° C., to this was added 2-bromo-4-tert-butylbenzaldehyde (4.06 g, 16.8 mmol)(prepared according to J. Med. Chem. 2005, 48, 71-90) in anhydrous THF (10 ml) at 0° C. The reaction mixture was stirred at ambient temperature for 3 hours. The mixture was quenched with saturated ammonium chloride solution and extracted with EtOAc. The combined solution was washed with brine, dried over sodium sulfate and concentrated in vacuo to give the crude product. The crude product was purified by column chromatography on silica gel, eluting with hexane, to afford the title compound (3.27 g, 81%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622589B2
Source datasetuspto-grants-2009_11
ORD IDord-07c7565ee8124b8db930fefbc750e56f
Source noteuspto-grants-2009_11