HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508490Generated: October 28, 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → 5-Methoxy-1H-inden-1-one
https://huagongshe.com/reaction/508490
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 3-Bromo-5-methoxy-2,3-dihydro-1H-inden-1-one | HCID 23250651 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Methoxy-1H-inden-1-one | HCID 11040990 | — |
Reaction Steps
DBU (9.2 mL, 61.7 mmol) was added to a solution of 5-methoxy-3-bromo-1-indanone (14.8 g, 61.7 mmol) in THF (100 mL) at −10° C. dropwise over 10 minutes. The resulting solution was stirred at −10° C. for 20 minutes, quenched via addition of saturated aqueous NH4Cl (100 mL), and extracted with EtOAc (3×100 mL). The combined organic extracts were washed with brine (100 mL), dried over MgSO4, and concentrated. The crude product was purified by column chromatography (SiO2) using a 0-35% ethyl acetate-hexanes gradient to afford 5.4 g (55%−two steps) of the subtitle compound. 1H NMR (CDCl3 300 MHz) δ 7.42 (d, 1H), 7.38 (d, 1H), 6.62 (s, 1H), 6.60 (d, 1H), 5.89 (d, 1H), 3.85 (s, 3H) ppm. MS calculated for C10H8O2+H: 161, observed: 161.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096520B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-6b08de69bd4a427390afc70215211971 |
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| Source note | uspto-grants-2015_08 |
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