Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546279Generated: November 1, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 5-Methoxy-1H-inden-1-one

https://huagongshe.com/reaction/546279

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant3-Bromo-5-methoxy-2,3-dihydro-1H-inden-1-oneHCID 23250651—
SolventTetrahydrofuranHCID 8028—
Product5-Methoxy-1H-inden-1-oneHCID 11040990—

Reaction Conditions

Temperature-10 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935830B2
Source datasetuspto-grants-2011_05
ORD IDord-39c3ea3b0d764e4b86e141384ba214d1
Source noteuspto-grants-2011_05