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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522876Generated: October 30, 2026

HCID 67355957, compound → HCID 58046537, compound

https://huagongshe.com/reaction/522876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67355957HCID 67355957—
CatalystZincHCID 23994—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 58046537HCID 5804653742%

Reaction Steps

To a stirred solution of 1-ethyl-1′-methylspiro[indoline-3,4′-piperidin]-2-one (0.0046 mol) in toluene (41.6 mL) was added 2,2,2 trichloro ethyl chloroformate (6.23 mL, 0.046 mol) at 0° C. and the reaction mixture was heated at reflux for 18 h. Progress of the reaction was monitored by TLC. The reaction mixture was cooled to RT, diluted with EtOAc (2×50 mL) and washed with water (2×12 mL) and brine (12 mL). The organic portions were combined, dried over Na2SO4 and evaporated under reduced pressure. The crude product was taken up in acetic acid (12.0 mL) and Zn (4.1 g, 0.062 mol) and was added portion wise at 0° C. The reaction mixture was allowed to stir at RT for 1 h. Progress of the reaction was monitored by TLC. The reaction mixture was filtered through Celite® (diatomaceous earth) and washed with EtOAc (2×20 mL), basified using saturated NH4OH solution (15.0 mL) and extracted with DCM (2×40 mL). the organic portions were combined, dried over Na2SO4 and evaporated under reduced pressure to obtain crude 1-ethylspiro[indoline-3,4′-piperidin]-2-one (42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334269B2
Source datasetuspto-grants-2016_05
ORD IDord-d2a33710d40f472ca0e67535d14c38ae
Source noteuspto-grants-2016_05