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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 380426Erstellt: 25. Oktober 2026

Potassium Hydroxide → HCID 22663183, Verbindung

https://huagongshe.com/reaction/380426

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
EduktCyclohexane, (bromomethyl)-HCID 137636—
EduktMethyl 3-methyl-1H-indole-6-carboxylateHCID 21938240—
KatalysatorSodium IodideHCID 5238—
LösungsmittelAcetoneHCID 180—
ProduktHCID 22663183HCID 2266318363%

Reaktionsschritte

A mixture of methyl 3-methyl-1 H-indole-6-carboxylate(10 g, Reference Example 30), cyclohexylmethylbromide (19 g), potassium hydroxide (12 g) and sodium iodide (0.1 g) in acetone (200 ml) was stirred at room temperature for 6 hours. The reaction mixture was evaporated. The residue was partitioned between ethyl acetate (250 ml) and water (250 ml). The aqueous layer was extracted three times with ethyl acetate (250 ml). The total combined organic phases were dried over sodium sulphate then evaporated. The residue was subjected to flash column chromatography on silica eluting with a mixture of ethyl acetate and hexane (gradient elution, 0:10 to 1:9, v/v)to yield the title compound (9.5 g). NMR (CDCl3): δ0.90-1.10(m), 1.10-1.40(m), 1.60-1.90(m), 2.30(s), 3.90-4.00(m), 3.90(s), 7.00(s), 7.50-7.60(m), 7.70-7.80(m), 8.00(s). MH+271.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06303600B1
Quelldatensatzuspto-grants-2001_10
ORD IDord-7d9d4ebb1263494bbb467a40ad157ad8
Quellennotizuspto-grants-2001_10