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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397501Generated: November 1, 2026

Trifluoroacetic acid → 5-(4-Bromophenyl)-4-oxa-1-azabicyclo[3.2.1]octane

https://huagongshe.com/reaction/1397501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 87560978HCID 87560978—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product5-(4-Bromophenyl)-4-oxa-1-azabicyclo[3.2.1]octaneHCID 68750368—

Reaction Conditions

Temperature40 °C

Reaction Steps

To an ambient solution of Example 54D (0.100 g, 0.186 mmol) in dichloromethane (1 mL) was added trifluoroacetic acid (0.5 ml). The reaction was stirred for 0.5 h, and the solution was then carefully added to a slurry of K2CO3 (3.0 g, 21.7 mmol) 1 h dichloromethane (10 mL). After the evolution of gas ceased, the mixture was heated to 40° C. for 1 h. The mixture was cooled to room temperature and was diluted with water (10 mL). The layers were separated, and the aqueous was extracted with additional dichloromethane (2×10 mL). The combined organic layers were dried with anhydrous Na2SO4, filtered, and concentrated under reduced pressure to give the title product, which was used in the subsequent step without further purification. MS (ESI) m/z 268 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901152B2
Source datasetuspto-grants-2014_12
ORD IDord-fcdcc581cdb44e5ab68dfbd06ea2bd8d
Source noteuspto-grants-2014_12