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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2199473Erstellt: 24. Oktober 2026

Cyclohexane → HCID 86730041, Verbindung

https://huagongshe.com/de/reaction/2199473

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclohexaneHCID 8078—
EduktSodium BicarbonateHCID 516892—
Edukt(S)-(-)-1-Amino-2-(methoxymethyl)pyrrolidineHCID 7156993—
Edukt6-iodo-3,4-dihydronaphthalen-1(2H)-oneHCID 45489800—
Katalysatorp-Toluenesulfonic acid monohydrateHCID 521998—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 86730041HCID 8673004198,7%

Reaktionsschritte

To a stirred mixture of 6-iodo-3,4-dihydronaphthalen-1(2H)-one (I-8A, 20.90 g, 77 mmol), p-toluenesulfonic acid monohydrate (0.584 g, 3.07 mmol), and cyclohexane (40 mL) was added (S)-2-(methoxymethyl)pyrrolidin-1-amine (10 g, 77 mmol) dropwise at room temperature under nitrogen. The mixture was heated with azeotropic removal of water for 5 h. The reaction mixture was diluted with ethyl acetate (20 mL) and mixed with saturated aqueous sodium bicarbonate solution (15 mL). The aqueous layer was separated and extracted with ethyl acetate (2×30 mL). The combined organic solutions were dried over anhydrous sodium sulfate and concentrated under reduced pressure. Flash chromatography purification (330 g silica gel column, gradient elution from 0% to 20% EtOAc in hexanes) afforded (S)—N-(6-iodo-3,4-dihydronaphthalen-1(2H)-ylidene)-2-(methoxymethyl)pyrrolidin-1-amine (29.1 g, 76 mmol) as a yellow liquid. LC/MS M+1=385.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09359286B2
Quelldatensatzuspto-grants-2016_06
ORD IDord-1445f10207fe4433a9bd0f756acc0296
Quellennotizuspto-grants-2016_06