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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromomethyl 3-methoxyphenyl ketone | HCID 101294 | — |
| 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 67265133 | HCID 67265133 | 97.8% |
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
| 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-f2ca54c6884740d8be4d1c38dd206d92 |
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| Source note | uspto-grants-2012_04 |
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