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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729471Generated: November 1, 2026

Iodoethane → HCID 67820205, compound

https://huagongshe.com/reaction/1729471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 67820261HCID 67820261—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67820205HCID 67820205103.4%

Reaction Steps

Under a nitrogen atmosphere in a round-bottom flask were placed 50 ml (0.12 mmol) of cis-5-(N-tert-butoxycarbonyl-2-methoxybenzylamino)-2-oxo-6-phenylpiperidine and 0.2 mL of THF. To the system were added 13.5 mg (0.12 mmol) of potassium tert-butoxide and 20 μL (0.24 mmol) of ethyl iodide. The reaction mixture was stirred at room temperature for 3 hours (during this period, additional potassium tert-butoxide (13.5 mg) and ethyl iodide (20 μL) were added to the system). The mixture was partitioned between methylene chloride and aqueous sodium bicarbonate, the layers were separated and the aqueous phase was extracted with three portions of methylene chloride. The combined organic fractions were dried (sodium sulfate) and concentrated with a rotary evaporator. The crude material was purified by flash column chromatography using 3:97 methanol/chloroform as the eluant to obtain 42 mg of cis-N-ethyl-5-(2-methoxybenzylamino)-2-oxo-6-phenylpiperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05332817
Source datasetuspto-grants-1994_07
ORD IDord-3fef08bbe2464b8e97016ad0d8b183c8
Source noteuspto-grants-1994_07