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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602526Generated: November 1, 2026

Hydrochloric Acid → 5-isopropyl-2-methyl-benzaldehyde

https://huagongshe.com/reaction/602526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
Reactant2-Bromo-p-cymeneHCID 137600—
ReactantHCID 178418306HCID 178418306—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product5-isopropyl-2-methyl-benzaldehydeHCID 5215589—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 2-bromo-4-isopropyl-1-methyl-benzene (863 mg, 4.0 mmol) in 10 mL of THF is added a solution of t-BuLi (1.7 M in pentane, 4.7 mL) dropwise at below −70° C. After addition, the reaction mixture is stirred at −78° C. for one hour. A solution of DMF (0.46 mL) in 1 mL of THF is added at the same temperature and stirred for additional one hour. The reaction mixture is allowed to warm to room temperature then poured into a mixture containing ice (50 g) and concentrated HCl (2 mL) and stirred for 15 minutes. To the mixture, ethyl ether (20 mL) is added. The organic layer is separated and the aqueous layer is extracted with ethyl ether. The organic solutions are combined, washed with brine, dried and concentrated to give 600 mg of 5-isopropyl-2-methyl-benzaldehyde. 1H NMR: (CDCl3) 10.27 (s, 1H), 7.66 (d, 1H), 7.34 (d, 1H), 7.17 (d, 1H), 2.94 (m, 1H), 2.63 (s, 3H), 1.24 (d, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906528B2
Source datasetuspto-grants-2011_03
ORD IDord-8f45e2cdb74f4aa0b82996b750f5487a
Source noteuspto-grants-2011_03