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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1910483Erstellt: 27. Oktober 2026

1,2-Dichloroethane → Bis(4-chlorophenyl)methyl quinuclidine-3-carboxylate

https://huagongshe.com/reaction/1910483

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
Edukt4,4'-DichlorobenzhydrolHCID 7033—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt1-Azabicyclo(2.2.2)octane-3-carboxylic acid hydrochlorideHCID 12673436—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktBis(4-chlorophenyl)methyl quinuclidine-3-carboxylateHCID 7092582427,9%

Reaktionsschritte

Quinuclidine-3-carboxylic acid hydrochloride (150 mg, 0.78 mmol), EDC (225 mg, 1.17 mmol) and HOBT (180 mg, 1.17 mmol) were dissolved in dry THF (7.5 ml). Bis(4-chlorophenyl)methanol (218 mg, 0.86 mmol) was added followed by TEA (382 μl, 2.74 mmol). The resulting reaction was stirred at room temperature overnight. THF was removed under vacuum, and the crude was partitioned between EtOAc and water. The organic phase was washed with sat. NaHCO3, dried over sodium sulphate, filtered, and evaporated to dryness. The crude was purified by flash chromatography (EtOAc/MeOH=8/2 to 7:3+1% of NH4OH) to obtain bis(4-chlorophenyl)methyl quinuclidine-3-carboxylate (85.0 mg, racemic mixture).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08604015B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-5946ae15d1684747a1fe17c1f788fb08
Quellennotizuspto-grants-2013_12