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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279240Generated: October 30, 2026

Isoquinoline-4-carbaldehyde → (Isoquinolin-4-yl)methanol

https://huagongshe.com/reaction/279240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoquinoline-4-carbaldehydeHCID 10868870—
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
SolventTetrahydrofuranHCID 8028—
Product(Isoquinolin-4-yl)methanolHCID 12746377—

Reaction Steps

4-Isoquinolinecarboxaldehyde (1 mmole) (prepared by the method of: J. B. Wommack, T. G. Barbee, Jr., D. J. Thoennes, M. A. McDonald and D. E. Pearson, J. Heterocyclic Chem., 1969, 6, 243-245.) is dissolved in anhydrous THF (50 mL) and treated with borane-methyl sulfide (0.3 mmoles) (as described in: E. Mincione, J. Org. Chem., 1978, 43, 1829-1830) at 0° C. for 0.5-1 h and worked up in the usual way to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362188B1
Source datasetuspto-grants-2002_03
ORD IDord-577be0b0b84a42acb9d78e31bd6f4cc8
Source noteuspto-grants-2002_03