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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068307Generated: October 25, 2026

Cyclohexane → 2-Chloro-N,N-diethyl-6-(trimethylgermyl)benzamide

https://huagongshe.com/reaction/1068307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexaneHCID 8078—
ReactantChlorotrimethylgermaneHCID 73723—
Reactant2-Chloro-N,N-diethylbenzamideHCID 82566—
ReactantAcetone cardiceHCID 18522661—
ReactantCID 53628100HCID 178418400—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-N,N-diethyl-6-(trimethylgermyl)benzamideHCID 1863004445%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 1.3M s-BuLi in cyclohexane (21.8 mL, 28.3 mmol) was added dropwise to a dry ice/acetone cooled solution of the compound of example e (4.6 g, 21.7 mmol) in THF (60 mL), maintaining the internal reaction temperature ≦−65° C. This mixture was stirred at −78° C. for 45 min, then was quenched by the dropwise addition of a solution of trimethylchlorogermane (5.0 g, 32.6 mmol) in THF (30 mL), again maintaining the internal reaction temperature ≦−65° C. The reaction was warmed to 0° C., diluted with ether, and extracted with 10% HCl (2×) followed with sat aq NaHCO3. The ether was dried (MgSO4), concentrated, and purified by HPLC with 6% EtOAc in hexanes to afford 3.2 g of the title compound as a white solid, a 45% yield. m.p. 47-48° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248894B1
Source datasetuspto-grants-2001_06
ORD IDord-ec5bbc6943f543c88df4fd7ccbaeb70c
Source noteuspto-grants-2001_06