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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1411313Generated: October 29, 2026

Water → HCID 90449655, compound

https://huagongshe.com/reaction/1411313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiethyl MalonateHCID 7761—
ReactantSodium hydrideHCID 24758—
ReactantHCID 90449442HCID 90449442—
SolventDimethylformamideHCID 6228—
ProductHCID 90449655HCID 9044965541.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

Sodium hydride (10.0 mg, 0.21 mmol) was dissolved in N,N-dimethylformamide (1 mL). Thereafter, diethyl malonate (13.0 μL, 0.086 mmol) was added to the above obtained solution under cooling on ice, and the thus obtained mixture was then stirred at 100° C. for 30 minutes. Thereafter, an N,N-dimethylformamide (0.5 mL) solution of 1-(2-(trimethylsilyl)ethyl) 1′-tert-butyl 5-(3-bromo-2-(bromomethyl)propyl)spiro[indoline-3,3′-pyrrolidine]-1,1′-dicarboxylate (51.1 mg, 0.080 mmol) was further added to the reaction solution under cooling on ice, and the thus obtained mixture was then stirred at 100° C. for 2 hours. Thereafter, water was added to the reaction solution, and the mixed solution was then extracted with ethyl acetate. The organic layer was washed with brine, and was then dried over anhydrous sodium sulfate, followed by concentration in vacuo. The obtained residue was purified by silica gel column chromatography (hexane ethyl acetate=5:1) to obtain 1-(2-(trimethylsilyl)ethyl) 1′-tert-butyl 5-((3,3-bis(ethoxycarbonyl)cyclobutyl)methyl)spiro[indoline-3,3′-pyrrolidine]-1,1′-dicarboxylate (20.8 mg, 41%) in the form of a colorless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921576B2
Source datasetuspto-grants-2014_12
ORD IDord-4e28e183cbdc4cd281fb59ac2d053486
Source noteuspto-grants-2014_12