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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1962416Generated: October 31, 2026

Benzyl Alcohol → HCID 58525656, compound

https://huagongshe.com/reaction/1962416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
ReactantHCID 58525647HCID 58525647—
Catalystpalladium(II) acetateHCID 167845—
ProductHCID 58525656HCID 5852565636.5%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of palladium acetate (21 mg, 0.095 mmol), 4,5-bis-diphenylphosphanyl-9,9-dimethyl-9H-xanthene (=Xantphos, 55 mg, 0.095 mmol), sodium carbonate (303 mg, 2.86 mmol), 4-bromo-8-fluoro-3-methyl-2-oxazol-2-ylmethyl-2H-isoquinolin-1-one (321 mg, 0.952 mmol), and benzyl alcohol (0.297 mL, 2.87 mmol) in toluene (3 mL, 30 mmol) was stirred under an atmosphere of carbon monoxide (P=3 bar) at 110° C. overnight. LC/MS indicated the formation of the title product and its benzyl ester (8-fluoro-3-methyl-2-oxazol-2-ylmethyl-1-oxo-1,2-dihydro-isoquinoline-4-carboxylic acid benzyl ester) in ca. 1:1 ratio. The reaction mixture was dissolved in 5 ml of ethanol, filtered through a short plug of celite and evaporated. It was partitioned between ethyl acetate (50 ml) and 0.5M aq. NaOH (2×25 ml). The combined aqueous solution was acidified with conc. aq. HCl, extracted with ethyl acetate (40 ml), the organic phase was washed with brine, dried (MgSO4) and evaporated to give 105 mg of the title product, yield 36.5%. LC-MS (m/z) 303.3 (MH+), tR=0.57.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415373B2
Source datasetuspto-grants-2013_04
ORD IDord-50dd64eec9da4c199a6e4a8f32450fcb
Source noteuspto-grants-2013_04