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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966281Generated: October 30, 2026

Triethylamine → 5-Hydroxymethyl-6-(2-trifluoromethylsulfonyloxyphenyl)-2,2,4-trimethyl-1,2-dihydroquinoline

https://huagongshe.com/reaction/1966281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoromethanesulfonyl chlorideHCID 79000—
Reactant5-Hydroxymethyl-6-(2-hydroxyphenyl)-2,2,4-trimethyl-1,2-dihydroquinolineHCID 57990610—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product5-Hydroxymethyl-6-(2-trifluoromethylsulfonyloxyphenyl)-2,2,4-trimethyl-1,2-dihydroquinolineHCID 5848548242%

Reaction Conditions

Temperature0 °C

Reaction Steps

5-Hydroxymethyl-6-(2-hydroxyphenyl)-2,2,4-trimethyl-1,2-dihydroquinoline (Reference Compound No. 3-1, 293 mg, 0.992 mmol) was dissolved in anhydrous dichloromethane (5 mL) and then triethylamine (167 μL, 1.20 mmol) and trifluoromethanesulfonyl chloride (106 μL, 0.996 mmol) were added thereto at 0° C. After the reaction mixture was stirred at 0° C. for 1 hour, it was diluted with chloroform (20 mL). The whole was washed with saturated aqueous NaHCO3 solution (20 mL) and then the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give the titled reference compound (177 mg) as an orange solid. (Yield 42%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420635B2
Source datasetuspto-grants-2013_04
ORD IDord-9142c59a4b8b492588dbf42d369b923d
Source noteuspto-grants-2013_04