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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 483406Erstellt: 25. Oktober 2026

Benzal chloride → Ethyl 1-(p-chlorobenzyl)-5-chloro-3-thiophenylindole-2-carboxylate

https://huagongshe.com/reaction/483406

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzal chlorideHCID 7411—
EduktAmmonium ChlorideHCID 25517—
EduktEthyl 5-chloro-3-thiophenylindole-2-carboxylateHCID 67902874—
EduktPotassium hexamethylsilamideHCID 131717145—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelTolueneHCID 1140—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexamethylphosphoramideHCID 12679—
ProduktEthyl 1-(p-chlorobenzyl)-5-chloro-3-thiophenylindole-2-carboxylateHCID 67855865—

Reaktionsschritte

To a cold (-78°), stirred solution containing 664 mg of ethyl 5-chloro-3-thiophenylindole-2-carboxylate from Preparation 5 in 3.5 mL of dry tetrahydrofuran, under argon, was added 3.5 mL of a 0.62 M solution of potassium hexamethylsilamide in toluene. The reaction mixture was stirred at -78° for 1 h and at 0° for 1 h then recooled to -78°. 0.75 mL of g chlorobenzyl chloride, 1.0 mL of hexamethylphosphoric triamide and 20 mg of tetra-n-butylammonium bromide were then added. The resultant mixture was allowed to warm to room temperature and stirred for 18 h. Saturated aqueous ammonium chloride and ether were added. The ether layer was separated, washed with water, 10% aqueous cupric sulfate, water and brine and dried over MgSO4.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05225421
Quelldatensatzuspto-grants-1993_07
ORD IDord-c149c78e537a4b2aaf0a44152e4574ab
Quellennotizuspto-grants-1993_07