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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188120Generated: October 30, 2026

Chlorotrimethylsilane → HCID 18630136, compound

https://huagongshe.com/reaction/2188120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantCyclohexaneHCID 8078—
ReactantHCID 18630045HCID 18630045—
ReactantCID 53628100HCID 178418400—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18630136HCID 1863013611.5%

Reaction Conditions

Temperature-100 °C

Reaction Steps

A solution of 1.3M s-BuLi in cyclohexane (16.15 mL, 21 mmol) was added dropwise to an ether/liquid N2 cooled (−100° C.) solution of N-ethyl-2-chloro-3-thiophenecarboxamide (1.90 g, 10 mmol) and TMEDA (3.17 mL, 21 mmol) in THF (100 mL). After stirring for 30 min at −100° C., TMSCl (2.28 g, 21 mmol) was added in a single portion. The resulting reaction mixture was warmed to −25° C. over 1 h, quenched with dilute aq citric acid, and extracted with EtOAc (3×). The combined organic extracts were dried (MgSO4), concentrated, and purified by HPLC with 3:17 EtOAc/hexanes to afford 0.3 g of the title compound as a white solid, an 11% yield. m.p. 46-48° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410558B1
Source datasetuspto-grants-2002_06
ORD IDord-c20878fe43ad4101a658f0831b2fd8ec
Source noteuspto-grants-2002_06