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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255381Generated: October 29, 2026

Triethylamine → HCID 66774573, compound

https://huagongshe.com/reaction/255381

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-BromoethanolHCID 10898—
ReactantDichloromethane methanolHCID 21226129—
ReactantHCID 66774485HCID 66774485—
SolventAcetonitrileHCID 6342—
ProductHCID 66774573HCID 6677457365%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of N,N-dibenzyl-2-methylpiperidin-4-amine (Intermediate 217, 880 mg, 3.0 mmol) in acetonitrile (6 mL) was added triethylamine (0.85 ml, 6.0 mmol) and 2-bromoethanol (0.32 mL, 4.5 mmol). The reaction is stirred at 70° C. at 300 watts in the microwave for 20 minutes. Acetonitrile was removed under reduced pressure, the residue was taken up in dichloromethane (100 mL) and saturated aqueous sodium hydrogen carbonate solution (30 mL) and the aqueous phase was back extracted three times with dichloromethane (3×70 mL). The combined organic phases were dried over sodium sulfate and concentrated to dryness under reduced pressure. Chromatography of the residue on silica gel with dichloromethane/methanol (10:1) gave 660 mg (65% yield) of the product as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875715B2
Source datasetuspto-grants-2011_01
ORD IDord-af82a60c7ce54df18e975fcd85d0ec4e
Source noteuspto-grants-2011_01