HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522876Generated: October 30, 2026
HCID 67355957, compound → HCID 58046537, compound
https://huagongshe.com/reaction/522876
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 67355957 | HCID 67355957 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58046537 | HCID 58046537 | 42% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09334269B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-d2a33710d40f472ca0e67535d14c38ae |
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| Source note | uspto-grants-2016_05 |
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