Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073160Generated: October 26, 2026

Tetrahydrofuran → Ethyl 2-methyl-4-(phenylmethyl)-1-piperazinecarboxylate

https://huagongshe.com/reaction/1073160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl chloroformateHCID 10928—
Reactant1-Benzyl-3-methylpiperazineHCID 2727520—
ReactantSodiumHCID 5360545—
SolventWaterHCID 962—
ProductEthyl 2-methyl-4-(phenylmethyl)-1-piperazinecarboxylateHCID 1472255387.8%

Reaction Steps

580 parts of a sodium bydroxide solution 1N in water were cooled in an ice bath and then there were added 44 parts of 3-methyl-1-(phenylmethyl)piperazine and 82.8 parts of tetrahydrofuran. A solution of 27.13 parts of ethyl carbonochloridate in 103.5 parts of tetrahydrofuran was added dropwise at a temperature at about 5° C. Upon completion, stirring was continued for 4 hours in an ice bath. The product was extracted with dichloromethane. The extract was washed with water, dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (99:1 by volume) as eluent. The pure fractions were collected and the eluent was evaporated, yielding 55 parts (87.8%) of ethyl 2-methyl-4-(phenylmethyl)-1-piperazinecarboxylate as a residue (int. 36).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968684
Source datasetuspto-grants-1990_11
ORD IDord-9f8544683bec4051b17e6e961906127d
Source noteuspto-grants-1990_11