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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598823Generated: November 1, 2026

Methanol → Isoquinoline-6-carboxaldehyde

https://huagongshe.com/reaction/598823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant6-VinylisoquinolineHCID 57950706—
SolventDichloromethaneHCID 6344—
ProductIsoquinoline-6-carboxaldehydeHCID 1529035994%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a 150 mL round-bottomed flask was added 6-vinylisoquinoline (2.47 g, 16 mmol) and MeOH (35 mL)/DCM (35 mL). The resulting solution was cooled to −78° C. The reaction was ozonized until a blue color persisted, then nitrogen gas was bubbled through the solution for 15 minutes to purge the ozone. The reaction was then treated with solid sodium bicarbarbonate. (1.5 g) and dimethyl sulfide (3.2 mL, 0.2 mL/mmol of SM) and the mixture was warmed to room temperature and stirred overnight. The reaction mixture was diluted with water (100 mL) and extracted with DCM (3×75 mL). The combined organic layers were dried over Na2SO4, filtered, and the residue product isoquinoline-6-carbaldehyde (2.35 g, 94% yield) was used without further manipulation. LCMS (API-ES) m/z (%): 158.1 (100%, M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897619B2
Source datasetuspto-grants-2011_03
ORD IDord-fd7334d1f8dd4f9791049e5168ac5b66
Source noteuspto-grants-2011_03