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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432890Generated: November 2, 2026

Hydrochloric Acid → 7-Chloroisoquinoline-3-carboxylic acid

https://huagongshe.com/reaction/1432890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
Reactant7-Chloroisoquinoline-3-carbaldehydeHCID 54145033—
CatalystSilver NitrateHCID 24470—
SolventWaterHCID 962—
Product7-Chloroisoquinoline-3-carboxylic acidHCID 17842395—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 4.5 mL of a 1N NaOH solution at 0° C. is added a solution of AgNO3 (0.31 g, 1.8 mmol) in 3 mL of H2O, followed by a solution of of 7-chloro-isoquinoline-3-carbaldehyde (0.25 g, 1.3 mmol) in 3 of EtOH. The solution is stirred at 0° C. for 10 minutes, then at room temp. For 3 hours. The solution is acidified to pH=3 with 1H HCl. The resulting solution is extracted with CHCl3. The organic layer is dried over MgSO4, filtered and concentrated to give the product as a white solid (0.2 g, 0.96 mmol). 1H NMR (CD3OD, 300 MHz) δ9.18 (s, 1H), 8.63 (s, 1H), 8.18 (m, 1H), 7.80 (m, 2H), 6.94 (m, 1H), 4.15 (q, 2H), 3.48 (s, 2H), 1.20 (t, 3H). MS (EI): m/z 208, 210 (M+), Cl pattern.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-6f0d52cd7acc4970b4e141bb8ee82b50
Source noteuspto-grants-2009_11