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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 1-Benzyl-3-methylpiperazine | HCID 2727520 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 2-methyl-4-(phenylmethyl)-1-piperazinecarboxylate | HCID 14722553 | 87.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04968684 |
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| Source dataset | uspto-grants-1990_11 |
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| ORD ID | ord-9f8544683bec4051b17e6e961906127d |
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| Source note | uspto-grants-1990_11 |
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