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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684911Generated: November 3, 2026

p-Chlorophenacyl bromide → HCID 44232240, compound

https://huagongshe.com/reaction/1684911

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Chlorophenacyl bromideHCID 68303—
ReactantSodium BicarbonateHCID 516892—
Reactant5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amineHCID 2756555—
Solvent1-PropanolHCID 1031—
ProductHCID 44232240HCID 44232240135.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

5.0 g of 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-ylamine and 5.30 g of 2-bromo-1-(4-chlorophenyl)ethanone are placed in 150 ml of n-propanol in a round-bottomed flask. 2.67 g of sodium hydrogencarbonate are added. The mixture is heated at 80° C. for 16 h. After cooling, the reaction mixture is concentrated under reduced pressure. 10.93 g of compound are obtained, which compound is used as is in the following stages.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148370B2
Source datasetuspto-grants-2012_04
ORD IDord-0be77c406661456ba60deb07698aad43
Source noteuspto-grants-2012_04