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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672734Generated: November 1, 2026

Lithium diisopropylamide → Trifluoro-methanesulfonic acid 3,5-dichloro-4-[1-(4,4-difluoro-cyclohexyl)-2-oxo-pyrrolidin-3-ylmethyl]-phenyl ester

https://huagongshe.com/reaction/1672734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 57878591HCID 57878591—
ReactantTrifluoro-methanesulfonic acid 3,5-dichloro-4-methanesulfonyloxymethyl-phenyl esterHCID 86634570—
SolventTetrahydrofuranHCID 8028—
ProductTrifluoro-methanesulfonic acid 3,5-dichloro-4-[1-(4,4-difluoro-cyclohexyl)-2-oxo-pyrrolidin-3-ylmethyl]-phenyl esterHCID 57878605—

Reaction Steps

To a solution of 1-(4,4-difluoro-cyclohexyl)-pyrrolidin-2-one (447 mg, 2.2 mmol) in 22 mL dry THF, add 1.76 mL of 2M LDA (1.2 eq.) in THF dropwise at −78° C. Then, add 1.24 g of trifluoro-methanesulfonic acid 3,5-dichloro-4-methanesulfonyloxymethyl-phenyl ester (1.4 eq) at −78° C. Allow the resulting solution to stand at room temp for overnight. Quench the mixture with saturated aqueous NH4Cl and extract with CH2Cl2. Wash the organic layer with water, then brine, and dry over Na2SO4, filter and concentrate. Purify the crude material by chromatography to afford the title compound: mass spectrum (m/z): 376 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998999B2
Source datasetuspto-grants-2011_08
ORD IDord-4077e4a8aafb471c9c02f11db51c5da0
Source noteuspto-grants-2011_08