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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990348Generated: October 30, 2026

Diethyl Ether → HCID 86758549, compound

https://huagongshe.com/reaction/990348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 11401906HCID 11401906—
ReactantHCID 18418679HCID 18418679—
SolventDimethylformamideHCID 6228—
ProductHCID 86758549HCID 8675854976.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

(S)-2-(Cyclohexyl-methyl-amino)-4-methyl-pentanoic acid (0.300 g, 1.32 mmol) was dissolved in dry DMF (4 mL) under nitrogen atmosphere and cooled to 0° C. in an ice-water bath. To this solution were added, in succession, N,N-diisopropylethylamine (0.690 mL, 3.96 mmol) and solid O-benzotriazol-1-yl-N,N,N,N′,N′-tetramethyluronium hexafluorophosphate (0.501 g, 1.32 mmol). The resulting reaction mixture was stirred at that temperature for 40 minutes; solid 4,4-bis-(4-fluoro-phenyl)-butylamine monohydrochloride (0.393 g, 1.32 mmol) was then added. After stirring for, sequentially, 15 minutes at 0° C. and 30 minutes at ambient temperature, reaction mixture was mixed with 60 mL of diethyl ether; the resulting mixture was successively washed with saturated aqueous NaHCO3 solution (2×60 mL), brine (2×60 mL), and was dried over Na2SO4. The solution was concentrated in vacuo affording an oil. The crude product was further purified by flash chromatography (50% EtOAc in hexane) and treated with ethereal HCl. Subsequent concentration in vacuo and drying under vacuum provided 0.51 g (75%) of the pure titled compound as a white foam; mp 73-83° C. APCI-MS m/z 471.4 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458781B1
Source datasetuspto-grants-2002_10
ORD IDord-1d61a42a51634b9280643aac2c7b5729
Source noteuspto-grants-2002_10