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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037668Generated: October 31, 2026

Iodoethane → HCID 44554169, compound

https://huagongshe.com/reaction/1037668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantTriethylamineHCID 8471—
ReactantHCID 44555334HCID 44555334—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 44554169HCID 44554169—

Reaction Conditions

Temperature40 °C

Reaction Steps

(3S)-3-[(S)-naphthalen-2-yl(2H-tetrazol-2-yl)methyl]piperidine (2.0 mmol) from Example 2 was dissolved in acetonitrile and the solution was treated with triethylamine (3.0 mmol) at room temperature. To this solution was added iodoethane in acetonitrile slowly and the solution was warmed up to 40° C. After the completion of the reaction, the reaction mixture was diluted with ethyl acetate, washed with 5% aq NaOH, water, brine, and dried over MgSO4. After concentration, the crude product was purified by flash column chromatography with a 10% Methanol in dichloromethane to afford (3S)-1-ethyl-3-[(S)-naphthalen-2-yl(2H-tetrazol-2-yl)methyl]piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546576B2
Source datasetuspto-grants-2013_10
ORD IDord-adaecb17aca24a608c59821e30bcc360
Source noteuspto-grants-2013_10