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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200384Generated: October 30, 2026

Acetic Acid → HCID 118105524, compound

https://huagongshe.com/reaction/2200384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1-(4-Fluorophenyl)piperazineHCID 75260—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 118119372HCID 118119372—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 118105524HCID 11810552485.9%

Reaction Steps

To a solution of (S)-ethyl 6-(3-oxocyclopentanecarboxamido)spiro[2.5]oct-5-ene-5-carboxylate (0.7 g, 2.23 mmol) in 1,2-dichloroethane (10 ml) were added 1-(4-fluorophenyl)piperazine (0.43 g, 2.40 mmol), glacial acetic acid (0.14 g, 2.40 mmol) and sodium triacetoxy borohydride (0.7 g, 3.44 mmol). The mixture was stirred at RT for 24 h before removal of the solvent. The residue was treated with saturated sodium bicarbonate, extracted with ethyl acetate and washed with brine. The organic layer was dried over sodium sulfate, filtered, and concentrated under reduced pressure to afford the crude residue which was purified by column chromatography over silica gel using ethyl acetate in hexane as eluents to obtain a diastereomeric mixture (7:3) of title compound (0.9 g, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359367B2
Source datasetuspto-grants-2016_06
ORD IDord-00f28658b3324f6fb605915371b1ec24
Source noteuspto-grants-2016_06