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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408236Generated: November 1, 2026

Methanol → Trifluoroacetic acid

https://huagongshe.com/reaction/1408236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 66588101HCID 66588101—
ReactantHCID 86709219HCID 86709219—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductTrifluoroacetic acidHCID 6422—
ProductHCID 86709218HCID 86709218—

Reaction Steps

To a solution of 2-(2-(3-(chloromethyl)benzamido)-5-(diethylamino)phenyl)-N-(3-(trifluoromethyl)benzyl)isonicotinamide 143a (715 mg, 1.2 mmol) and S-2,5,8,11,14,17,20,23-octaoxapentacosan-25-yl ethanethioate 135c.3 (590 mg, 1.33 mmol) in DMF (10 mL) was added 4.3 M NaOMe in MeOH (0.37 mL, 1.6 mmol) and stirred at room temperature for 15 minutes. The reaction mixture was added to water (35 mL) and extracted with DCM (3×50 mL). The combined organic layers were washed with water (25 mL), dried (Na2SO4) and concentrated at reduced pressure. The residue was purified by flash chromatography on silica gel (1% to 5% MeOH in DCM). The purified product was dissolved in 50% ACN/water and TFA (410 mg, 3.6 mmol) was added. Lyophylization gave a TFA salt of the title compound (1.34 g) as a light yellow oil. MS (ES, m/z): 959.4 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916569B2
Source datasetuspto-grants-2014_12
ORD IDord-26bc53ab6d23467c8bbdc532769dc84b
Source noteuspto-grants-2014_12