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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095076Generated: October 31, 2026

Acetic Acid → 3-Chloro-2-fluoro-6-methoxybenzaldehyde

https://huagongshe.com/reaction/1095076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethylformamideHCID 6228—
Reactant1-Chloro-2-fluoro-4-methoxybenzeneHCID 2724521—
ReactantLithium diisopropylamineHCID 45051747—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-Chloro-2-fluoro-6-methoxybenzaldehydeHCID 2213970785%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 4-chloro-3-fluoroanisole (10.2 g, 63.5 mmol, Oakwood) in tetrahydrofuran (100 mL) at −78° C. was added lithium diisopropyl amine (42.3 mL, 1.8 M in THF, 76.2 mmol) dropwise during a period of 15 min. The mixture was stirred at −78° C. for another 20 mins. Then N,N-dimethyl-formamide (5.9 mL, 76.2 mmol) was added in one portion. The mixture was stirred at −78° C. for 10 min, then quenched with acetic acid (15.6 g, 254 mmol) and followed by the addition of water (80 mL). The mixture was partitioned between ethyl acetate and water. The organic layer was separated, concentrated to give 3-chloro-2-fluoro-6-methoxy-benzaldehyde as a yellow solid (Yield: 10 g, 85%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134001B2
Source datasetuspto-grants-2012_03
ORD IDord-48e648302af648bd8c1c2e8bed33d01d
Source noteuspto-grants-2012_03