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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629209Generated: October 30, 2026

Trifluoroacetic acid → HCID 57516717, compound

https://huagongshe.com/reaction/629209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantTriethylsilaneHCID 12052—
ReactantHCID 58464056HCID 58464056—
SolventDichloromethaneHCID 6344—
ProductHCID 57516717HCID 5751671780%

Reaction Conditions

Temperature22.5 °C

Reaction Steps

(275 mg, 828 μmol) (5RS)-5-Hydroxy-1-(5-iodopyridin-2-yl)-4,4-dimethylpyrrolidin-2-one (Example 13, step 2) was dissolved in CH2Cl2 (2 ml) and trifluoroacetic anhydride (140 μl, 994 μmol, 1.2 equiv.) was added at room temperature. The mixture was stirred for 1 hr at 20-25° C. The solution was evaporated to dryness and the residue was dissolved in trifluoroacetic acid (957 μl, 12.4 mmol, 15 equiv.) and triethylsilane (159 μl, 994 μmol, 1.2 equiv.) was added at room temperature. The mixture was stirred 1 h at room temperature. The reaction mixture was evaporated and extracted with sat. NaHCO3 solution and two times with a small volume of dichloromethane. The crude product was purified by flash chromatography by directly loading the dichloromethane layers onto a silica gel column (20 gr, ethyl acetate/heptane gradient, 0:100 to 100:0). The desired 1-(5-iodopyridin-2-yl)-4,4-dimethylpyrrolidin-2-one (209 mg, 80% yield) was obtained as a white solid, MS: m/e=317.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315498B2
Source datasetuspto-grants-2016_04
ORD IDord-f8f498810cd443b09999acea5f9c0bce
Source noteuspto-grants-2016_04