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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188154Generated: October 29, 2026

Hexachloroethane → HCID 18630338, compound

https://huagongshe.com/reaction/2188154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexachloroethaneHCID 6214—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantCyclohexaneHCID 8078—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 4300248HCID 4300248—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18630338HCID 1863033886.9%

Reaction Conditions

Temperature-78 °C

Reaction Steps

1.3 M s-BuLi in cyclohexane (41 mL, 0.053 mol) as added dropwise to a solution of the above amide (5 g, 0.024 mol) and TMEDA (4 ml, 0.027 mol) in THF, cooled to −78° C. under nitrogen. After 30 min a solution of hexachloroethane (6.4 g, 0.027 mol) in THF was added. After 0.5 h at −78° C. the reaction mixture was warmed to −30° C. and poured into dilute aq NaHCO3 and extracted with ether. The ether extract was washed with water and brine, dried (MgSO4) and concentrated. The resulting solid was recrystallized from cyclohexane to give 5 g of 2-chloro-4-t-butyl-N-ethylbenzamide, a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410558B1
Source datasetuspto-grants-2002_06
ORD IDord-6ddc52dd0b8c4e68ad79fc14342696ad
Source noteuspto-grants-2002_06