HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684911Generated: November 3, 2026
p-Chlorophenacyl bromide → HCID 44232240, compound
https://huagongshe.com/reaction/1684911
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Chlorophenacyl bromide | HCID 68303 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine | HCID 2756555 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | HCID 44232240 | HCID 44232240 | 135.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08148370B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-0be77c406661456ba60deb07698aad43 |
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| Source note | uspto-grants-2012_04 |
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