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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1941352Erstellt: 26. Oktober 2026

Isocaproaldehyde → N-Butyl-gamma-hydroxy-alpha-methyl-delta-[(4-methylpentyl)amino]cyclohexanehexanamide hydrochloride

https://huagongshe.com/reaction/1941352

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsocaproaldehydeHCID 129—
EduktDichloromethaneHCID 6344—
EduktSodium BicarbonateHCID 516892—
EduktSodium triacetoxyborohydrideHCID 5049666—
Eduktdelta-Amino-N-butyl-gamma-hydroxy-alpha-methyl-cyclohexanehexanamideHCID 19908509—
LösungsmittelAcetic AcidHCID 176—
ProduktAmmonium HydroxideHCID 14923—
ProduktN-Butyl-gamma-hydroxy-alpha-methyl-delta-[(4-methylpentyl)amino]cyclohexanehexanamide hydrochlorideHCID 6768462759%

Reaktionsschritte

To a solution of [αS-(αR*,γR*,δR*)]δ-amino-N-butyl-γ-hydroxy-α-methyl-cyclohexanehexanamide (II: 0.17 g, 0.57 mmol) and 4-methylvaleraldehyde (0.063 g, 0.63 mmol) in CH2Cl2 (3 mL) was added NaBH(OAc)3 (0.181 g, 0.86 mmol) and glacial acetic acid (0.05 mL). The mixture was stirred at r.t. for 16 h. The reaction was made basic (pH=8) by the addition of sat aqueous NaHCO3 and extracted with CH2Cl2. The organic extracts were washed with brine, dried (Na2SO4), filtered and concentrated in vacuo. Silica gel chromatography (19:19:1 0.05 CHCl3 :Et2O:MeOH:NH4OH) of the concentrate gave the free amine (0.128 g, 59%) which was converted to its hydrochloride salt by the addition of 1.5N ethanolic HCl (0.3 mL). Removal of solvent in vacuo gave the title compound (0.128 g, 59%) as an amorphous white solid, mp 65° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05703129
Quelldatensatzuspto-grants-1997_12
ORD IDord-55726ee26f674e34a300e2287dac8cae
Quellennotizuspto-grants-1997_12