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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695909Generated: October 31, 2026

Triethylamine → Benzyl 3-oxo-2,3-dihydrospiro[indene-1,4'-piperidine]-1'-carboxylate

https://huagongshe.com/reaction/1695909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
ReactantSpiro[indene-1,4'-piperidin]-3(2H)-one hydrochlorideHCID 18673582—
SolventDichloromethaneHCID 6344—
ProductBenzyl 3-oxo-2,3-dihydrospiro[indene-1,4'-piperidine]-1'-carboxylateHCID 5943337699%

Reaction Steps

To a solution spiro[indene-1,4′-piperidin]-3(2H)-one hydrochloride (5.0 g, 24.84 mmol) and Et3N (7.54 g, 74.53 mol) in CH2Cl2 (50 mL) was added drop-wise Cbz-Cl (4.66 g, 27.33 mmol) at 0° C. The reaction was allowed to warm to room temperature and stirred overnight. The precipitate was filtered, washed with Et2O and dried to furnish benzyl 3-oxo-2,3-dihydrospiro[indene-1,4′-piperidine]-1′-carboxylate (6.1 g, yield 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163737B2
Source datasetuspto-grants-2012_04
ORD IDord-2840ae1457bc4dab946ff52219988d1d
Source noteuspto-grants-2012_04