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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375025Generated: November 4, 2026

Triethylamine → HCID 17963842, compound

https://huagongshe.com/reaction/1375025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant2-Amino-2-methyl-1-propanolHCID 11807—
Reactant3-IODO-5-TRIFLUOROMETHYLBENZOIC ACIDHCID 15648617—
SolventDichloromethaneHCID 6344—
ProductHCID 17963842HCID 17963842—

Reaction Conditions

Temperature-30 °C

Reaction Steps

To a solution of 3-iodo-5-(trifluoromethyl)benzoic acid (2.32 g) and triethylamine (1.13 ml) in dichloromethane (20 ml) was added dropwise a solution of ethyl chloroformate (1.4 ml) in dichloromethane (2.0 ml) over 10 minutes at −30° C., and the mixture was stirred at −30° C. for 1 hour. 2-Amino-2-methyl-1-propanol was added dropwise to the mixture over 5 minutes at −30° C., and the mixture was stirred at −30° C. for 30 minutes and then at room temperature for 1 hour. The mixture was quenched with aqueous ammonium chloride solution at 0° C., and extracted with dichloromethane (X2). The combined organic extracts were washed successively with saturated aqueous sodium hydrogen carbonate solution, 1N hydrochloric acid and brine, and then dried over magnesium sulfate, evaporated, and purified with column chromatography (silica gel, ethyl acetate:hexane=20:80) to give N-(2-hydroxy-1,1-dimethylethyl)-3-iodo-5-(trifluoromethyl)benzamide (2.10 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166598B2
Source datasetuspto-grants-2007_01
ORD IDord-84078714ba7a464d93a776d250321bd5
Source noteuspto-grants-2007_01