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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235291Generated: October 31, 2026

Tetrahydrofuran → HCID 59299517, compound

https://huagongshe.com/reaction/2235291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 59299333HCID 59299333—
ReactantHCID 178418255HCID 178418255—
ProductHCID 59299517HCID 592995179%

Reaction Steps

Dissolve 3-chloro-4-((1-cyclohexyl-2-oxopyrrolidin-3-yl)methyl)benzonitrile (0.20 g, 0.63 mmol) in THF (20 mL) under N2 and add phenylmagnesium bromide (0.63 mL, 0.63 mmol, 1.0 M in THF). Stir the reaction mixture for 24 hours until LC-MS shows the starting material has gone. Add saturated NH4Cl (20 mL) and extract the aqueous with EtOAc (3×50 mL). Combine the organic layers and dry with Na2SO4, filter, concentrate and purify by flash column chromatography (silica gel, 20-50% of EtOAc-Hexane) to give 0.023 g (9%) of the title compound as white solid: MS (APCI-pos mode) m/z (rel intensity) 396.3 (100), 398.2 (30).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713979B2
Source datasetuspto-grants-2010_05
ORD IDord-45ab8028a31f48068c93ea89e27dbc94
Source noteuspto-grants-2010_05