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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571600Generated: October 31, 2026

HCID 89979039, compound → HCID 58383065, compound

https://huagongshe.com/reaction/571600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 89979039HCID 89979039—
CatalystPalladiumHCID 23938—
CatalystZincHCID 23994—
SolventPropan-2-one--water (1/1)HCID 18366337—
ProductHCID 58383065HCID 5838306586.7%

Reaction Steps

Bdb was synthesized according to FIG. 15. Briefly, 1-iodo-5-methylanisole (100 mg, 0.4 mmol) was added in to a mixture of 10% Pd on carbon (100 mg) and zinc powder (100 mg, 1.5 mmol) suspended in 5.2 mL of acetone/water (1:1), and the mixture was stirred at room temperature overnight. The solution was extracted with diethyl ether and the ether layer was collected and dried over anhydrous Na2SO4. The ether was removed under reduced pressure and the residue was applied to a flash column chromatography to afford 2,2′-dimethoxy-4,4′-dimethyl biphenyl as a yellow solid (42 mg, 46%). The conversion of 2,2′-dimethoxy-4,4′-dimethyl biphenyl to 4,4′-bis-bromomethyl-2,2′-dimethoxy-biphenyl was accomplished by following a previously reported procedure and resulted in a 31% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029332B2
Source datasetuspto-grants-2015_05
ORD IDord-5871256ff8d3433fafc4e5a2f45ae2b6
Source noteuspto-grants-2015_05