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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523739Generated: October 27, 2026

Methanol → 4-Hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid butyl ester

https://huagongshe.com/reaction/523739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium AcetateHCID 517045—
ReactantButyl 1-bromo-4-hydroxy-7-phenoxyisoquinoline-3-carboxylateHCID 86595463—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product4-Hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid butyl esterHCID 6671295177.1%

Reaction Steps

A mixture of 208 mg of 1-Bromo-4-hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid butyl ester (0.5 mmol), 49 mg of sodium acetate (0.6 mmol), 50 mg of 10 wt % palladium on charcoal, 10 ml of methanol, and 5 ml of ethyl acetate was stirred under hydrogen at 1 atm for 15 h. Then the mixture was filtered by suction through a pad of celite and was concentrated in vacuo. The residue was partitioned between 2 ml of half concentrated aqueous bicarbonate solution and 8 ml of ethyl acetate. The organic phase was dried over MgSO4. Evaporation in vacuo gave 130 mg of the title compound; 1H NMR (CDCl3): δ=11.89 (bs, 1H), 8.61 (s, 1H), 8.36 (d, 1H), 7.10 to 7.53 (m, 7H), 4.49 (t, 2H), 1.87 (m, 2H), 1.47 (m, 2H), 0.98 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09339527B2
Source datasetuspto-grants-2016_05
ORD IDord-d7c29f7863a341c79d732b5383974350
Source noteuspto-grants-2016_05