HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088161Generated: November 1, 2026
Water → (1R*,2R*,5R*)-2-{[3,5-Bis(trifluoromethyl)phenyl]methoxy}-8-(2-bromoacetyl)-1-phenyl-8-azabicyclo[3.2.1]octane
https://huagongshe.com/reaction/2088161
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | (1R*,2R*,5R*)-2-{[3,5-bis(trifluoromethyl)phenyl]methoxy}-1-phenyl-8-azabicyclo[3.2.1]octane | HCID 86586647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1R*,2R*,5R*)-2-{[3,5-Bis(trifluoromethyl)phenyl]methoxy}-8-(2-bromoacetyl)-1-phenyl-8-azabicyclo[3.2.1]octane | HCID 86586694 | — |
Reaction Steps
(1R*,2R*,5R*)-2-{[3,5-Bis(trifluoromethyl)phenyl]methoxy}-1-phenyl-8-azabicyclo[3.2.1]octane (Example 60; 162 mg, 0.38 mmol) was dissolved in THF (3 ml) and triethylamine (0.059 ml, 0.42 mmol) added. The reaction mixture was cooled to 0° C. then bromoacetyl bromide (0.037 ml, 0.42 mmol) added, then the mixture warmed to room temperature. A further 1.1 equivalents of triethylamine (0.059 ml), and bromoacetyl bromide (0.037 ml) were added and the reaction mixture stirred at room temperature for 15 minutes. The reaction mixture was poured into water, extracted with ethyl acetate (×3), dried (MgSO4), and concentrated in vacuo to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06727249B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-37d85fa153584b428cd7f35887b94f4f |
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| Source note | uspto-grants-2004_04 |
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