HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291998Generated: October 29, 2026
Water → 1-(2-bromophenyl)-3-(1H-pyrrol-2-yl)-2-propen-1-one
https://huagongshe.com/reaction/2291998
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyrrole-2-carboxaldehyde | HCID 13854 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2'-Bromoacetophenone | HCID 75060 | — |
| Solvent | Ethyl acetate methylcyclohexane | HCID 66985183 | — |
| Product | 1-(2-bromophenyl)-3-(1H-pyrrol-2-yl)-2-propen-1-one | HCID 53639365 | 75% |
Reaction Steps
A mixture of 20.0 g of (0.21 moles) 2-pyrrolecarboxaldehyde, 71.4 mL of (0.52 moles) o-bromoacetophenone, 72 mL of 1N potassium hydroxide and 800 mL of water was placed in a flask under nitrogen and heated to 45° C. for 72 hr. The reaction was cooled in an ice bath until a solid formed. The solid was taken up in methylcyclohexane/EtOAc, dried over 4A sieves and allowed to cool. The resulting solid was recrystallized from methylcyclohexane/EtOAc to give 43.5 g of 1-(2-bromophenyl)-3-(1H-pyrrol-2-yl)-2-propen-1-one as a yellow solid (75%), mp 76°-78° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04800207 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-816212b44ce941eda55c7a526d07d5aa |
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| Source note | uspto-grants-1989_01 |
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