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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015543Generated: November 1, 2026

Trifluoroacetic acid → HCID 67017828, compound

https://huagongshe.com/reaction/1015543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86761371HCID 86761371—
SolventDichloromethaneHCID 6344—
ProductHCID 67017828HCID 67017828120.5%

Reaction Steps

To a stirred solution of the compound obtained from step I (0.45 g, 1.12 mmol) in dichloromethane (1.1 mL) at 0° C. was added trifluoroacetic acid (1.1 mL). The reaction mixture was gradually warmed to room temperature and stirred for 1 h. The volatiles were removed under vacuum and the residue was triturated several times with diethyl ether to obtain 2-[(3-aminotricyclo[3.3.1.03,7]non-1-yl)methyl]-1H-isoindole-1,3(2H)-dione (0.4 g) as its trifluoroacetic acid salt in 86% yield. m/z (M+1) 297; 1H NMR (DMSO-d6) 300 MHz δ 8.05 (s (br), 2H), 7.92-7.80 (m, 4H), 3.51 (s, 2H), 2.38-2.30 (m, 1H), 2.30-2.22 (m, 1H), 1.85-1.66 (m, 6H), 1.60-1.50 (m, 3H), 1.45-1.38 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985759B2
Source datasetuspto-grants-2011_07
ORD IDord-b354505679b348a3b0e78798047c06dc
Source noteuspto-grants-2011_07