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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289820Generated: November 2, 2026

7-Chloromethyl-1,4-dichloro-isoquinoline → 4-chloro-7-(hydroxymethyl)-1(2H)-isoquinolone

https://huagongshe.com/reaction/2289820

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Chloromethyl-1,4-dichloro-isoquinolineHCID 18698312—
ReactantEthyl 4-chloro-1-oxo-1,2-dihydro-7-isoquinolinecarboxylateHCID 18698325—
SolventTetrahydrofuranHCID 8028—
Product4-chloro-7-(hydroxymethyl)-1(2H)-isoquinoloneHCID 1869843086%

Reaction Steps

7-(Chloromethyl)-1,4-dichloro-isoquinoline ##STR186## LiBH4 (530 mg, 24.3 mmol) was added portionwise to a stirred solution of ethyl 4-chloro-1-oxo-1,2-dihydro-7-isoquinolinecarboxylate (3.06 g, 12.2 mmol) in THF (100 mL) and the mixture was stirred at room temperature for 1 h. The heterogeneous mixture was quenched with dilute HCl (2 M), and extracted with CH2Cl7 (2×100 mL) and EtOAc (5×100 mL). The remaining solid was taken up in hot EtOH, and allowed to cool to yield a white fluffy solid. This solid was combined with the combined organic extracts, evaporated in vacuo and crystallised with EtOH to give 4-chloro-7-(hydroxymethyl)-1(2H)-isoquinolone (2.19 g, 10.49 mmol) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093731
Source datasetuspto-grants-2000_07
ORD IDord-8f71c2a4eb4345d680effc9fd3c5fda7
Source noteuspto-grants-2000_07