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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1887087Generated: November 3, 2026

Sodium Hydroxide → Isoquinoline, 5-chloro-6-fluoro-

https://huagongshe.com/reaction/1887087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantChlorosuccinimideHCID 31398—
Reactant6-FluoroisoquinolineHCID 21889847—
SolventSulfuric AcidHCID 1118—
ProductIsoquinoline, 5-chloro-6-fluoro-HCID 5981826158.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

7.0 g (38.1 mmol) of 6-Fluoroisoquinoline (23) are dissolved in 60 mL of concentrated sulfuric acid. At 0° C. 10.18 g of N-Chlorosuccinimide are added. After 1 h another 5.2 g of N-Chlorosuccinimide are added and the solution is warmed to 50° C. Two more portions of 5.2 g N-Chlorosuccinimide are added successively and stirring is continued at 50° C. until the reaction is complete. The reaction mixture is cooled to room temperature, is poured on ice and adjusted to pH 10 by addition of sodium hydroxide. The precipitate is filtered off, taken up in dichloromethane and washed with aqueous sodium hydroxide. The organic layer is dried over magnesium sulfate, evaporated and the crude product is purified by preparative HPLC to yield 4.04 g of 5-Chlor-6-fluor-isoquinoline (151) as trifluoroacetate. Rt=0.97 min (Method #2). Detected mass: 182.0/184.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501736B2
Source datasetuspto-grants-2013_08
ORD IDord-ac3e09ea33dc4782b85e3d7e18e8ef6a
Source noteuspto-grants-2013_08