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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752233Generated: October 27, 2026

Sodium hydride → Ethyl 5-fluoro-1-oxo-1,3-dihydrospiro[indene-2,4'-piperidine]-1'-carboxylate

https://huagongshe.com/reaction/1752233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant5-Fluoro-1-indanoneHCID 136537—
ReactantEthyl bis(2-bromoethyl)carbamateHCID 10924683—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductEthyl 5-fluoro-1-oxo-1,3-dihydrospiro[indene-2,4'-piperidine]-1'-carboxylateHCID 7122751632.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of 5-fluoro-1-indanone (302 mg, 2.013 mmol) and bis-(2-bromo-ethyl)-carbamic acid ethyl ester (610 mg, 2.01 mmol) in DMF (5 mL) at 50° C. was added NaH (121 mg, 5.03 mmol) by small portions. After being stirred at 50° C. for 16 hr, the reaction was cooled to 25° C. The reaction was diluted with 15 mL of ethyl acetate and washed twice with 10 mL of water, dried over Na2SO4 and concentrated in vacuo. The crude product was purified by flash column (gradient of 85:15 to 60:40 heptane/ethyl acetate in 20 min to give the title compound (188 mg, 0.645 mmol, 32.1% yield). MS (ESI) [m/e, (M+H)+]=292.4. HPLC retention time=1.46 minutes (Agilent 1100 HPLC system; 3.0 cm×3.0 mm×3.0 um C8 column; flow rate of 2.0 mL/min; gradient of 5-95% acetonitrile/water with 0.1% formic acid over 2 minutes).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09163003B2
Source datasetuspto-grants-2015_10
ORD IDord-1e64211d81be4628a0b5b4674fe24e5a
Source noteuspto-grants-2015_10