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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1423113Erstellt: 25. Oktober 2026

Formaldehyde → HCID 23627568, Verbindung

https://huagongshe.com/reaction/1423113

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt(S)-3-Benzyl-1-(3-cyclopentyloxy-4-methoxy-phenyl)-piperazineHCID 16725642—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 23627568HCID 23627568—

Reaktionsschritte

A solution of (S)-3-Benzyl-1-(3-cyclopentyloxy-4-methoxy-phenyl)-piperazine (73 mg, 0.20 mmol) in CH2Cl2 (5 mL) was treated with a 37% aqueous formaldehyde solution (16 μL, 0.22 mmol) and stirred for 5 min after which time solid sodium triacetoxyborohydride (64 mg, 0.30 mmol) was added. The suspension was then stirred for 3 hr then quenched with a saturated aqueous NaHCO3 solution (2 mL). The organic component was separated, dried over MgSO4, filtered, and evaporated to an oil which was purified by silica gel flash chromatography with 5% MeOH/CH2Cl2 as eluant to afford the title compound as a burgundy oil (69 mg, 91%). 1H NMR (CDCl3) 7.33-7.20 (m, 5H), 6.72 (d, J=8.6, 1H), 6.35 (d, J=2.9, 1H), 6.30 (dd, J=8.6, 2.9, 1H), 4.62-4.59 (m, 1H), 3.76 (s, 3H), 3.32-3.22 (m, 2H), 3.13-3.02 (m, 3H), 2.67-2.60 (m, 4H), 2.57 (s, 3H), 1.85-1.77 (m, 6H), 1.61-1.54 (m, 2H). 13C NMR 148.4, 146.1, 144.5, 139.0 (CH), 129.5 (CH), 128.6, 126.4 (CH), 113.2 (CH), 107.8 (CH), 106.2 (CH), 80.4 (CH), 63.7 (CH), 56.8 (CH3), 55.1 (CH2), 55.0 (CH2), 50.2 (CH2), 42.9 (CH3), 36.3 (CH2), 33.0 (CH2), 24.2 (CH2). LC/MS (Method A) 5.10 min, [M+1]+ 381.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08927546B2
Quelldatensatzuspto-grants-2015_01
ORD IDord-400df85a0cf24a66810af24cd8b0040f
Quellennotizuspto-grants-2015_01