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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421627Generated: November 2, 2026

1,2-Dimethoxyethane → HCID 54217329, compound

https://huagongshe.com/reaction/2421627

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium CarbonateHCID 10340—
ReactantMethyl 3-bromobenzoateHCID 12070—
ReactantHCID 67214057HCID 67214057—
CatalystHCID 178420554HCID 178420554—
SolventWaterHCID 962—
ProductHCID 54217329HCID 54217329—

Reaction Steps

Methyl 3-bromobenzoate (458 mg, 2 mmol), 1-styreneboronic acid pinacoyl ester (484 mg, 2.1 mmol), Na2CO3 (222 mg, 2.1 mmol), tetrakis(triphenylphosphino)palladium (116 mg, 0.1 mmol), water (4 mL) and 1,2-dimethoxyethane (6 mL) were stirred with reflux conditions for one hour, under nitrogen. The reaction mixture was diluted with water and was extracted three times with EtOAc. The organic layers were combined, washed with water and then brine, dried over MgSO4 and concentrated. The product was purified by trituration with Et2O. White crystals were obtained (393 mg, 82%). NMR 1H (ppm, CDCl3): 8.19 (t, J4=1.6 Hz, 1H), 7.91 (dt, J3=7.7 Hz, J4=1.3 Hz, 1H), 7.67 (d, J3=7.8 Hz, 1H), 7.52 (d, J3=7.3 Hz, 2H), 7.42 (t, J3=7.9 Hz, 1H), 7.36 (t, J3=7.4 Hz, 2H), 7.30-7.26 (m, 1H), 7.19 (d, J3=16.3 Hz, 1H), 7.11 (d, J3=16.4 Hz, 1H), 3.06 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956216B2
Source datasetuspto-grants-2011_06
ORD IDord-2a7b4def46c2476fbd538e9e13664739
Source noteuspto-grants-2011_06