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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069185Generated: October 31, 2026

Trifluoroacetic acid → HCID 68491403, compound

https://huagongshe.com/reaction/2069185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86643591HCID 86643591—
SolventDichloromethaneHCID 6344—
ProductHCID 68491403HCID 68491403100%

Reaction Steps

To a solution of 9 (560 mg, 2.2 mmol) in CH2Cl2 (15 mL) was added trifluoroacetic acid (15 mL). The reaction mixture was stirred at room temperature for 30 min. The solvent was removed by rotary evaporation. The yellow oil was put under vacuum for 24 h to give crude amine 4b (579 mg, 2.2 mmol, 100%) as a yellow oil, which was used in the next step without further purification: 1H NMR (500 MHz, CDCl3) δ 1.10-1.30 (br s, 1H), 1.40-1.60 (br s, 1H), 2.30-2.50 (br s, 1H), 2.70-2.90 (br s, 1H), 6.70-6.72 (m, 1H), 6.72-6.77 (m, 1H), 6.89-7.00 (m, 1H), 7.10-7.30 (m, 1H), 7.80-8.20 (br s, 2H), 10.8-11.8 (br s, 1H); 13C NMR (125 MHz, CDCl3) δ 13.2, 21.5, 31.6, 113.5, 113.7, 114.2, 114.4, 122.29, 122.31, 130.4, 130.5, 140.1, 140.2, 162.2, 164.1; LCQ-MS (M+H+) calcd for C9H11FN 152. found 152; LC-TOF (M+H+) calcd for C9H11FN 152.08755. found 152.08703.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299100B2
Source datasetuspto-grants-2012_10
ORD IDord-7ea981356d144f419a07326752cdfeed
Source noteuspto-grants-2012_10