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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728001Generated: November 3, 2026

Acetic Acid → 2,3-Difluoro-6-methylbenzaldehyde

https://huagongshe.com/reaction/1728001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethylformamideHCID 6228—
Reactant3,4-DifluorotolueneHCID 2733400—
ReactantLithium diisopropylamineHCID 45051747—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2,3-Difluoro-6-methylbenzaldehydeHCID 5756598957.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 1,2-difluoro-4-methyl-benzene (5.0 g, 39 mmol) in tetrahydrofuran (200 mL) at −78° C. was added lithium diisopropyl amine (24 mL, 1.8 M in THF, 43 mmol) dropwise during a period of 15 mins. The mixture was stirred at −78° C. for another 20 min. Then N,N-dimethyl-formamide (3.6 mL, 47 mmol) was added in one portion. The mixture was stirred at −78° C. for 10 min, then quenched with acetic acid (9.4 g, 1.56 mmol) and followed by the addition of water (37.6 mL). The mixture was partitioned between ethyl acetate and water. The organic layer was separated, concentrated. The residue was purified by chromatography (EtOAc:hexanes=1:1) to give 2,3-difluoro-6-methyl-benzaldehyde as colorless oil (Yield: 3.5 g, 57.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495007B2
Source datasetuspto-grants-2009_02
ORD IDord-c5e03d5665634ecda5cd2e5561acafe7
Source noteuspto-grants-2009_02