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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684916Generated: November 4, 2026

Bromomethyl 3-methoxyphenyl ketone → HCID 67265133, compound

https://huagongshe.com/reaction/1684916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethyl 3-methoxyphenyl ketoneHCID 101294—
ReactantSodium BicarbonateHCID 516892—
Reactant5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amineHCID 2756555—
Solvent1-PropanolHCID 1031—
ProductHCID 67265133HCID 6726513397.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

5.00 g of 2-bromo-1-(3-methoxyphenyl)ethanone and 4.80 g of 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-ylamine are placed in 220 ml of n-propanol in a round-bottomed flask and 2.57 g of sodium hydrogencarbonate are added. The mixture is heated at 80° C. for 20 h and allowed to cool. The reaction mixture is concentrated under reduced pressure. The residue is taken up between water and ethyl acetate, the organic phase is separated by settling and dried over magnesium sulphate and then the solvent is concentrated. 7.47 g of compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148370B2
Source datasetuspto-grants-2012_04
ORD IDord-f2ca54c6884740d8be4d1c38dd206d92
Source noteuspto-grants-2012_04