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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 375438Erstellt: 23. Oktober 2026

Triethylamine → HCID 56978006, Verbindung

https://huagongshe.com/de/reaction/375438

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt3-Indoleglyoxylyl chlorideHCID 89952—
Edukt(3aS,4S,7aS)-7,7-diphenyl-4-(2-methoxyphenyl)perhydroisoindol-4-ol hydrochlorideHCID 70218598—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 56978006HCID 5697800697,3%

Reaktionsschritte

A solution of 0.43 g of 2-(3-indolyl)-2-oxoacetyl chloride in 20 cm3 of dry dichloromethane and then a solution of 0.6 cm3 of triethylamine in 5 cm3 of dry dichloromethane are added in succession to a suspension of 0.96 g of (3aS,4S,7aS)-7,7-diphenyl-4-(2-methoxyphenyl)perhydroisoindol-4-ol hydrochloride in 25 cm3 of dry dichloromethane at room temperature, while stirring. The reaction mixture is stirred at this temperature for 24 hours, subsequently diluted with 200 cm3 of dichloromethane, washed with 100 cm3 of an aqueous 1N solution of sodium hydroxide and with 50 cm3 of an aqueous saturated solution of sodium chloride, and is dried over magnesium sulphate and concentrated to dryness under reduced pressure (2.7 kPa). The residue is chromatographed on a Merck silica gel column (particle size 0.04-0.06 mm, diameter 2.5 cm, height 1 cm) by eluting under a pressure of 0.4 bar of nitrogen with a mixture of 1,2-dichloroethane and methanol (70/30 by volume) and collecting fractions of 15 cm3. Fractions 2 to 9 are combined and concentrated to dryness under reduced pressure (2.7 kPa). 1.15 g of (3aS,4S,7aS)-7,7-diphenyl-2-[2-oxo-2-(3-indolyl)acetyl]-4-(2-methoxyphenyl)perhydroisoindol-4-ol are obtained in the form of an orange foam.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05484804
Quelldatensatzuspto-grants-1996_01
ORD IDord-06c4dca4b5eb4defb8c1dbf6a287d814
Quellennotizuspto-grants-1996_01