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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481332Generated: October 30, 2026

Piperazine → HCID 14988910, compound

https://huagongshe.com/reaction/481332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantEthanesulfonyl chlorideHCID 11667—
Reactant4-Nitrophenyl chloroformateHCID 82129—
Reactant4-(1,5-Dimethyl-1,2-epoxy-4-hexenyl)-5-methoxy-1-oxaspiro(2.5)octan-6-olHCID 219089—
SolventPyridineHCID 1049—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 14988910HCID 14988910—

Reaction Steps

A mixture of 6-hydroxy-5-methoxy-4-[2-methyl-3-(3-methyl-2-butenyl)oxiranyl]-1-oxaspiro[2,5]octane (400 mg), p-nitrophenyl chloroformate (570 mg) and pyridine (1.37 ml) in dichloromethane (6 ml) was stirred for 3 hours at ambient temperature and then piperazine (1.0 g) was added thereto. After stirring at ambient temperature for half an hour, the mixture was treated with ethanesulfonyl chloride (183 mg). The reaction mixture was stirred for 15 minutes at 0° C. and for 3 hours at ambient temperature. The resulting mixture was diluted with diethyl ether and washed with 1N HCl, 1N NaOH and brine. The organic layer was dried and concentrated in vacuo to give a crude oil which was purified by silica gel column chromatography to yield 6-[4-(ethanesulfonyl)piperazin-1-ylcarbonyloxy]-5-methoxy-4-[2-methyl-3-(3-methyl-2-butenyl)oxiranyl]-1-oxaspiro[2,5)octane as crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05789405
Source datasetuspto-grants-1998_08
ORD IDord-6effbe2e1ade49cbb680c717c9da90bc
Source noteuspto-grants-1998_08