HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372534Generated: November 1, 2026
1-Penten-3-one → 5-Amino-4-bromo-2-ethyl-2-(3-oxopentyl)-1-indanone
https://huagongshe.com/reaction/1372534
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Penten-3-one | HCID 15394 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 17972674 | HCID 17972674 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Amino-4-bromo-2-ethyl-2-(3-oxopentyl)-1-indanone | HCID 17972752 | 102% |
Reaction Steps
A solution of 5-(acetylamino)-4-bromo-2-ethyl-1-indanone (1.0 g, 3.39 mmol) in MeOH (5.1 mL) was treated with 0.5M NaOMe in MeOH (3.4 mL, 1.7 mmol) and ethyl vinyl ketone (0.506 mL, 5.08 mmol). The mixture was stirred and heated at 60° C. for 4.5 hours, then evaporated under vacuum. The residue was partitioned between EtOAc (75 mL), brine (50 mL), and water (10 mL). The organic portion was dried over MgSO4, filtered, and evaporated under vacuum. The residue was added to a short column of silica gel (30 mL) which was washed with CH2Cl2 (150 mL) and eluted with EtOAc (150 mL). The EtOAc eluant was evaporated under vacuum to provide crude 5-amino-4-bromo-2-ethyl-2-(3-oxopentyl)-1-indanone (1.17 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157604B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-f306aa7ddea34de68a7af81adb81b4f8 |
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| Source note | uspto-grants-2007_01 |
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