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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238360Generated: October 30, 2026

Sodium Carbonate → HCID 68685783, compound

https://huagongshe.com/reaction/2238360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium HydroxideHCID 14798—
ReactantOxalic acid dihydrateHCID 61373—
ReactantTolylboronic acidHCID 79799—
ReactantHCID 68683499HCID 68683499—
Catalystpalladium(II) acetateHCID 167845—
SolventDichloromethaneHCID 6344—
ProductHCID 68685783HCID 68685783—

Reaction Steps

6,7-dimethoxy-1-(4′-methyl-biphenyl-4-ylmethyl)-1,2,3,4-tetrahydro-isoquinoline oxalate (36) was prepared as follows: 1-(4-bromo-benzyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinoline hydrochloride (0.452 g, 1 mmol) was added to a mixture of 20 mL CH2Cl2 and 20 ml of 1N NaOH. The reaction mixture was stirred at room temperature. After dissolving of precipitate organic phase was separated, dried over Na2SO4, filtered and evaporated. A residue was dissolved in 6 mL i-PrOH. 4-Methyl-phenyl-boronic acid (0.148 g, 1.09 mmol) was added. The resulting solution was stirred for 30 min at room temperature. Pd(OAc)2 (1 mg, 0.0045 mmol), PPh3 (7 mg, 0.0267 mmol) and 2N Na2CO3 (1 mL, 2 mmol) were added, the reaction mixture was refluxed for 6 h under Ar and evaporated. A residue was dissolved in chloroform and washed with 1N NaOII. Organic phase was dried under Na2SO4, filtered and evaporated. A residue was dissolved in MeOH, a solution of oxalic acid dihydrate (0.265 g, 2.1 mmol) was added under reflux. Oxalic acid salt was crystallized from MeOH-Et2O mixture. Yield is 0.219 g (47.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718672B2
Source datasetuspto-grants-2010_05
ORD IDord-9150e64f6a9a48839802baf309f1a90f
Source noteuspto-grants-2010_05