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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371016Generated: October 30, 2026

Hydrochloric Acid → 4-(Bromomethyl)benzaldehyde

https://huagongshe.com/reaction/1371016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisobutylaluminum hydrideHCID 14487—
Reactant4-(Bromomethyl)benzonitrileHCID 86996—
ReactantTetrahydrofuran tolueneHCID 22635083—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product4-(Bromomethyl)benzaldehydeHCID 11206421—

Reaction Steps

To a THF-toluene (2.4 L-0.24 L) solution of α-bromo-p-tolunitrile (266.4 g, 1.36 mol) maintained at an internal temperature bellow 0° C. was added DIBAL in hexane (1.0 M) (1.49 L, 1.49 mol) over a period of 2 h. After a period of 1.5 h, the reaction mixture was transferred via canula to a 3N HCl solution (8 L) at 0° C. To the resulting suspension EtOAc (4 L) and THF (0.8 L) were added. After stirring, the organic phase was separated and evaporated to give a yellow solid. The solid was stirred in 20% EtOAc in hexane (1.3 L) for 3 hours. After filtration and drying the title compound was obtained. (210 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583126B2
Source datasetuspto-grants-2003_06
ORD IDord-06d06c91adf0402692dceed32bceabaa
Source noteuspto-grants-2003_06