HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354328Generated: October 27, 2026
4-Bromophenacyl bromide → 1-(4-Bromophenyl)-2-(1-pyrrolidinyl)ethanone
https://huagongshe.com/reaction/2354328
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Bromophenacyl bromide | HCID 7454 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(4-Bromophenyl)-2-(1-pyrrolidinyl)ethanone | HCID 21383095 | 96% |
Reaction Steps
2-bromo-1-(4-bromophenyl)ethanone (5.0 g, 18 mmol) was dissolved in 10 mL diethyl ether and added dropwise over 15 min to a solution of pyrrolidine (3.0 mL, 36 mmol) in 20 mL diethyl ether cooled to 0° C. in an ice bath. The resulting solution was allowed to warm to room temperature and maintained for 1 h. The solvent was removed under reduced pressure. The residue was dissolved in 100 mL of EtOAc and washed with sodium bicarbonate (100 mL) and then brine (100 mL). The organic layer was dried over Na2SO4, filtered, and concentrated under reduced pressure to give 4.6 g (96%) of the title compound as a yellow/orange solid. MS (ES) m/e 268/270 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07749998B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-29b3e73253d842a1af650f83bebb1ca4 |
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| Source note | uspto-grants-2010_07 |
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