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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349718Generated: October 30, 2026

Triethylamine → HCID 87870259, compound

https://huagongshe.com/reaction/349718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 131726274HCID 131726274—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 87870259HCID 87870259—

Reaction Steps

1-(3,5-bis(trifluoromethyl)benzyloxy)-4-amino-2-phenylbutan-2-ol TFA salt (37 mg, 0.071 mmol) was dissolved in 1,2-dichloroethane (0.6 ml). Triethylamine (0.040 ml, 0.29 mmol) was added to the solution, and followed by addition of trifluoroacetic anhydride (0.013 ml, 0.091 mmol) and catalytic amount of 4-dimethylaminopyridine. After stirred overnight at room temperature, the reaction mixture was concentrated, and the residue was purified by flash chromatography on silica gel to give the desired trifluoroacetamide. 1H NMR (300 MHz, Acetone) δ ppm 8.27 (s, 1 H) 7.95 (s, 2 H) 7.94 (s, 1 H) 7.54–7.61 (m, 2 H) 7.31–7.40 (m, 2 H) 7.23–7.31 (m, 1 H) 4.72–4.84 (m, 2 H) 4.69 (s, 1 H) 3.73–3.84 (m, 2 H) 3.29–3.43 (m, 1 H) 3.19 (ddd, J=19.39, 8.05, 5.86 Hz, 1 H) 2.27 (ddd, J=8.60, 6.40, 4.39 Hz, 2 H); LRMS [ESI, MNa+] m/z calcd for C21H18NO3F9Na 526.10, found 525.97.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179926B2
Source datasetuspto-grants-2007_02
ORD IDord-9f10c1e2c7af42ec946fe01ceb477152
Source noteuspto-grants-2007_02