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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186163Generated: November 3, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 76831218, compound

https://huagongshe.com/reaction/1186163

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant4-Acetamidobenzenesulfonyl azideHCID 5129185—
ReactantHCID 58562927HCID 58562927—
SolventTetrahydrofuranHCID 8028—
ProductHCID 76831218HCID 7683121892%

Reaction Conditions

Temperature23 °C

Reaction Steps

To a solution of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) (4.2 ml, 28 mmol) in THF (24 ml) at 23° C. was added a solution of (5-bromo-2-fluoro-phenyl)-acetic acid allyl ester (intermediate B3A) (7.29 g, 27 mmol) and commercially available p-acetamidobenzenesulfonyl azide ([CAS No. 2158-14-7], 6.94 g, 28 mmol) in THF (48 ml) over 1 h. The mixture was stirred for 5 h at 23° C. Then it was quenched with sat. aqueous ammonium chloride solution, diluted with ethyl acetate, and the organic layer was washed with brine and dried over sodium sulfate. Removal of the solvent in vacuum left a yellow oil, which was purified by silica gel column chromatography with hexane/ethyl acetate to give the title compound as a yellow solid (7.344 g, 92%). MS (ISP): m/z=316.1 [(M+NH4)+] and 318.0 [(M+2+NH4)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673894B2
Source datasetuspto-grants-2014_03
ORD IDord-eb7c45a62350436590fcf24dbc9e9407
Source noteuspto-grants-2014_03