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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647070Generated: November 1, 2026

Dichloromethane → HCID 14888694, compound

https://huagongshe.com/reaction/1647070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantHCID 14888693HCID 14888693—
ReactantHCID 131717728HCID 131717728—
SolventEthyl AcetateHCID 8857—
ProductHCID 14888694HCID 1488869486.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 8.30 g (0.026 mol) of rac.-2-acetamido-3-[3-hydroxyphenyl)propanoic acid benzyl ester and 10.0 g (0.028 mol) of N-phenyl-N-trifluoromethyl 1,1,1-trifluoromethyl sulfonyl sulfonamide in 110 mL of freshly distilled dichloromethane was cooled in an ice bath and 4.10 mL (0.029 mol) of triethylamine was added dropwise. The resulting mixture was stirred 1 hour at 0° C. and was allowed to warm to room temperature over 2 hours. The mixture was diluted with 250 mL of ethyl acetate and was washed with successive 50 mL portions of water, 1N sodium hydroxide, 1N hydrochloric acid, water, and brine and was dried over magnesium sulfate. Filtration and concentration afforded an oil which was purified by preparative chromatography on a Waters Prep 500 liquid chromatograph fitted with two Prep-Pak silica gel cartridges, eluting with 40% ethyl acetate-hexane to give 10.02 g (85%) of rac.-2-acetamido-3-[3-[(trifluoromethylsulfonyl)oxy]phenyl]propanoic acid benzyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05182263
Source datasetuspto-grants-1993_01
ORD IDord-fbf10e91cc164ea29cc9561f6dff134f
Source noteuspto-grants-1993_01