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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 909309Generated: November 1, 2026

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

https://huagongshe.com/reaction/909309

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 numberUS08017775B2
Source datasetuspto-grants-2011_09
ORD IDord-363e7c4ce3414164848876eec1a24e02
Source noteuspto-grants-2011_09