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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159364Generated: November 3, 2026

Trifluoroacetic acid → HCID 178511301, compound

https://huagongshe.com/reaction/1159364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 178453658HCID 178453658—
SolventDichloromethaneHCID 6344—
ProductHCID 178511301HCID 17851130191%

Reaction Steps

Trifluoro-acetic acid (3.5 mL, 49 mmol) was added to a solution of Example 38, tert-butyl ({trans-3-[4-(pyrrolidin-1-ylmethyl)phenoxy]cyclobutyl}methyl)carbamate (2.16 g, 6 mmol) in dichloro-methane (20 mL). The reaction mass was stirred at room temperature for 2 h and evaporated in vacuo. The residue was diluted with water (50 mL), and the obtained solution was extracted with CH2Cl2. The organic layer was discarded. The aqueous one was alkalized with 10 N NaOH to pH 12 and extracted with CHCl3 (3×50 mL). The combined extracts were dried and evaporated to afford the title compound (1.4 g, 91%) as a yellow oil. LCMS-data: M+H 261.2, 262.2 (calc 260.38). 1H NMR-data (DMSO-d6): 7.17 (d, 2H, Ph, J=8.6 Hz); 6.72 (d, 2H, Ph, J=8.6 Hz); 4.65-4.76 (m, 1H); 3.47 (s, 3H, CH2); 2.63 (d, 2H, CH2, J=6.6 Hz); 2.32-2.42 (m, 4H); 2.18-2.28 (m, 3H); 2.00-2.13 (m, 2H); 1.60-1.72 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812040B2
Source datasetuspto-grants-2010_10
ORD IDord-eb150da7bfd34af69da7c11e6edef792
Source noteuspto-grants-2010_10