HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619529Generated: November 2, 2026
Phenacyl bromide → (3R)-3-(2-(tert-butoxycarbonylamino)-2-(4-chlorophenyl)acetoxy)-1-(2-oxo-2-phenylethyl)-1-azoniabicyclo[2.2.2]octane bromide
https://huagongshe.com/reaction/1619529
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | HCID 67607091 | HCID 67607091 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (3R)-3-(2-(tert-butoxycarbonylamino)-2-(4-chlorophenyl)acetoxy)-1-(2-oxo-2-phenylethyl)-1-azoniabicyclo[2.2.2]octane bromide | HCID 86665838 | 42.1% |
Reaction Steps
2-Bromo-1-phenylethanone (55.4 mg, 0.28 mmol) was added to a solution of (R)-quinuclidin-3-yl 2-(tert-butoxycarbonylamino)-2-(4-chlorophenyl)acetate (C47) (100 mg, 0.25 mmol) in EtOAc (3 ml). The reaction was stirred at RT for 36 hours, and then a second portion of 2-bromo-1-phenylethanone (50.4 mg, 0.25 mmol) was added, and the reaction was stirred at RT for additional 48 hours. The organic phase was washed with aq. Na2CO3, dried over Na2SO4 and evaporated. The crude was dissolved in acetonitrile (3 ml), and 2-bromo-1-phenylethanone (60.0 mg, 0.30 mmol) was added. The reaction was heated under microwave irradiation at 100° C. for 45 minutes. The solvent was evaporated and the crude was purified by flash chromatography (DCM/MeOH=95/5 to 9/1) to obtain (3R)-3-(2-(tert-butoxycarbonylamino)-2-(4-chlorophenyl)acetoxy)-1-(2-oxo-2-phenylethyl)-1-azoniabicyclo[2.2.2]octane bromide (62.5 mg; 42% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08772314B2 |
|---|
| Source dataset | uspto-grants-2014_07 |
|---|
| ORD ID | ord-5f13bec1cb574863af09edd93fd20d8b |
|---|
| Source note | uspto-grants-2014_07 |
|---|