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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 4-Acetamidobenzenesulfonyl azide | HCID 5129185 | — |
| Reactant | HCID 58562927 | HCID 58562927 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 76831218 | HCID 76831218 | 92% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08673894B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-eb7c45a62350436590fcf24dbc9e9407 |
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| Source note | uspto-grants-2014_03 |
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