Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943159Generated: November 2, 2026

(5,6,7,8-Tetrahydroisoquinolin-3-yl)methanol → 5,6,7,8-Tetrahydroisoquinoline-3-carbaldehyde

https://huagongshe.com/reaction/1943159

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5,6,7,8-Tetrahydroisoquinolin-3-yl)methanolHCID 18799805—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product5,6,7,8-Tetrahydroisoquinoline-3-carbaldehydeHCID 1879957877.1%

Reaction Steps

A solution of 5,6,7,8-tetrahydro-3-isoquinolinylmethanol (572 mg, 3.50 mmol) in (DCM) (10 ml) at rt under argon was treated with manganese dioxide (3.047 g, 35.0 mmol) and then stirred at rt for 2 h. The reaction mixture was then filtered through a thin pad of Kieselguhr, eluting with DCM (50 ml), the organic extracts were evaporated to give the crude product as a brown oil (435 mg, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389524B2
Source datasetuspto-grants-2013_03
ORD IDord-b19c5a977e604a02bf151ce9f30ee29f
Source noteuspto-grants-2013_03