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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368690Generated: October 26, 2026

Hydrochloric Acid → 2-Chloro-N-ethyl-6-(1,1-dimethylethyl)benzamide

https://huagongshe.com/reaction/368690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexachloroethaneHCID 6214—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant2-tert-butyl-N-ethylbenzamideHCID 18630043—
ReactantCID 53628100HCID 178418400—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventCyclohexaneHCID 8078—
Product2-Chloro-N-ethyl-6-(1,1-dimethylethyl)benzamideHCID 18630210—

Reaction Conditions

Temperature-30 °C

Reaction Steps

To a solution of 2-tert-butyl-N-ethylbenzamide (44 g, 215 mmol) and TMEDA (70 mL, 446 mmol) in 500 mL THF at -70° C. under a positive nitrogen atmosphere was added at a rapid stream 520 mL 1.3M s-BuLi in cyclohexane, maintaining the temperature at below -60° C. After the addition was complete, the resulting reaction solution was warmed to -30° C. and stirred at between -30° C. and -26° C. for 50 min. The solution was then cooled to below -70° C. and a solution of hexachloroethane (80 g) in 250 mL THF was added at between -70 and -65° C. Stirring at below -70° C. was continued for 0.5 h. The resulting reaction solution was then poured into water. CH2Cl2 and 3N HCl were added. The aq layer was separated and extracted with CH2Cl2. The combined organic layers were washed with water, dried and concentrated in vacuo. The solid was triturated with hexane and then purified by flash chromatography with 15% ethyl acetate/hexane as eluent to give the desired product as a white solid. m.p. 121-123° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06133252
Source datasetuspto-grants-2000_10
ORD IDord-b7c1152e897747faafbb455667ae8c49
Source noteuspto-grants-2000_10