HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170737Generated: October 30, 2026
1-Indanone, 4-bromo- → HCID 117665512, compound
https://huagongshe.com/reaction/2170737
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Indanone, 4-bromo- | HCID 98713 | — |
| Reactant | Methyl 4-(bromomethyl)benzoate | HCID 256687 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 117665512 | HCID 117665512 | 4.4% |
Reaction Steps
A solution of lithium diisopropylamide (2.0 M in THF, 2.5 mL, 5.0 mmol) was added to a solution of 4-bromo-2,3-dihydro-1H-inden-1-one (4-bromo-1-indanone, 960 mg, 4.55 mmol) in THF (9.1 mL) at −78° C. After 1 h at −78° C., a solution of methyl 4-(bromomethyl)benzoate (1.25 g, 5.46 mmol) in THF (5 mL) was added via cannula. The reaction mixture was allowed to warm to room temperature naturally. After stirring at room temperature overnight, the reaction was quenched with saturated aqueous NH4Cl (50 mL) and extracted with EtOAc (3×100 mL). The combined organic extracts were dried (Na2SO4), filtered and concentrated. The resulting crude residue was purified by combiflash (330 g column, hexanes→30% EtOAc/hexanes, gradient) to afford 72 mg (4%) of methyl 4-((4-bromo-1-oxo-2,3-dihydro-1H-inden-2-yl)methyl)benzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051294B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-f98460ab604d41f8b0d0177e7774ddf8 |
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| Source note | uspto-grants-2015_06 |
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