Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 529101Generated: October 30, 2026

HCID 86651805, compound → HCID 69809727, compound

https://huagongshe.com/reaction/529101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86651805HCID 86651805—
ReactantHCID 178478191HCID 178478191—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69809727HCID 6980972768.1%

Reaction Steps

To a stirred solution of (3S,5′S)-tert-butyl 5′-(methoxy(methyl)carbamoyl)-2-oxospiro[indoline-3,3′-pyrrolidine]-1′-carboxylate (310 mg, 0.826 mmol) in THF (4 mL) was added 4-chloro phenylmagnesium bromide (1.0 N in THF, 2.89 mL, 2.89 mmol) at about 0° C. The reaction mixture was warmed to about room temperature and stirred overnight. The reaction was quenched with saturated aqueous NH4Cl solution and extracted with EtOAc. The combined organic layers were washed with brine, dried and concentrated. The crude product was purified by column chromatography (hexanes:EtOAc, 1:1) to give (3S,5′S)-tert-butyl 5′-(4-chlorobenzoyl)-2-oxospiro[indoline-3,3′-pyrrolidine]-1′-carboxylate (0.240 g, 68%). LCMS (APCI+) m/z 427, 429 [M+H]+; Rt=3.94 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346805B2
Source datasetuspto-grants-2016_05
ORD IDord-b3d2fb4553a246bb97c847f7d17ea371
Source noteuspto-grants-2016_05