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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054886Generated: November 1, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 2-(4-bromophenyl)-3,6-dihydro-2H-pyran

https://huagongshe.com/reaction/1054886

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant4-bromo-2-(4-bromophenyl)tetrahydro-2H-pyranHCID 69654381—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product2-(4-bromophenyl)-3,6-dihydro-2H-pyranHCID 8669886162.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 4-bromo-2-(4-bromophenyl)tetrahydro-2H-pyran (320 mg, 1.00 mmol) in toluene (5 mL) was added 1,8-Diazabicyclo[5.4.0]undec-7-ene (304 mg, 2.00 mmol). The mixture was stirred at 100° C. for 16 hours. The mixture was then diluted with ethyl acetate and water. The organic layer was washed with brine, dried over sodium sulfate, filtered and concentrated. The residue was purified by silica gel chromatography to give the title compound (150 mg) which contained some impurity of 4-bromobenzaldehyde. 1H NMR (400 MHz, CDCl3) δ ppm 7.48 (d, 2H) 7.30 (d, 2H) 5.92 (m, 1H) 5.82 (m, 1H) 4.52 (dd, 1H) 4.36 (m, 2H) 2.27 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394285B2
Source datasetuspto-grants-2016_07
ORD IDord-0c5c68c2425549ef94aa163e2d9f1b74
Source noteuspto-grants-2016_07