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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090465Generated: October 27, 2026

Sulfuric Acid → 6-Fluoro-7-bromoisoquinoline

https://huagongshe.com/reaction/2090465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus oxide (P4O10)HCID 14812—
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
Reactant3-Bromo-4-fluorobenzaldehydeHCID 173604—
SolventTolueneHCID 1140—
Product6-Fluoro-7-bromoisoquinolineHCID 5340296418.5%

Reaction Steps

A reaction mixture of 3-bromo-4-fluorobenzaldehyde (1.70 g, 8.37 mmol) and aminoacetaldehyde dimethyl acetal (0.917 mL, 8.37 mmol) in toluene (17.0 mL) was stirred at r.t. overnight. Then sulfuric acid (10 mL) and phosphorus pentoxide (2.38 g, 8.37 mmol) were added. The mixture was stirred at 160° C. for 1 h. After cooled, the mixture was poured into crushed ice. The acidic mixture was carefully adjusted to pH=8 by the addition of aqueous NaOH solution (1 N) with stirring and external cooling. The mixture was extracted with ethyl acetate (3×200 mL). The combined organic layers were washed with brine, dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was purified by flash chromatography on a silica gel column with 40% ethyl acetate in hexanes to afford the desired product (0.35 g, 18.5%). LCMS (M+H)+: m/z=225.9/227.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436008B2
Source datasetuspto-grants-2013_05
ORD IDord-3ba6d717fbb64ac3b6664a50dd94cf03
Source noteuspto-grants-2013_05