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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46116Generated: October 30, 2026

Trifluoroacetic acid → HCID 58930118, compound

https://huagongshe.com/reaction/46116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 58930151HCID 58930151—
CatalystWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 58930118HCID 5893011895.9%

Reaction Steps

To a 100 mL round-bottomed flask equipped with magnetic stirring was added tert-butyl 4-(4-(methylsulfonyl)phenyl)bicyclo[2.2.2]octan-1-ylcarbamate (170 mg, 448 μmol), 2 mL of CH2Cl2, ca. 5 drops of water, and trifluoroacetic acid (2 mL, 27 mmol). The reaction mixture was stirred at ambient temperature for 3.5 h, after which time the mixture was concentrated in vacuo. NaOH (ca. 50 mL of a 1M aq. solution) was added to the mixture, and the aqueous layer was extracted with CH2Cl2 (3×15 mL). The organic layers were combined, dried over K2CO3, filtered, and concentrated in vacuo to give 4-(4-(methylsulfonyl)phenyl)bicyclo[2.2.2]octan-1-amine (mass=120 mg, Mass Spec. m/z+ion=280.2) The crude reaction product was taken onto the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541592B2
Source datasetuspto-grants-2013_09
ORD IDord-0fba3511840847b6a6a07beef2097e36
Source noteuspto-grants-2013_09