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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401684Generated: October 29, 2026

N-Fluorobenzenesulfonimide → 3-Fluoro-5-phenyl-benzo[b]thiophene-2-carboxylic acid

https://huagongshe.com/reaction/401684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-FluorobenzenesulfonimideHCID 588007—
Reactant5-Phenylbenzo[b]thiophene-2-carboxylic acidHCID 59626071—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-Fluoro-5-phenyl-benzo[b]thiophene-2-carboxylic acidHCID 5962582572.3%

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a solution of compound 52c (507 mg, 1.99 mmol) in THF (8 mL) at −70° C. was added n-BuLi (1.6 M in hexane, 2.62 mL, 4.19 mmol). The mixture was stirred at −70° C. for 1 h; then a solution of N-fluorobenzenesulfonimide (817.3 mg, 2.59 mmol) in THF (2 mL) was slowly added. The reaction mixture was allowed to warm to room temperature and was stirred overnight. The resulting mixture was partitioned between dilute aqueous HCl and EtOAc. The organic solution was washed with water and brine, dried over Na2SO4, and concentrated. The residue was tritrated from CH2Cl2, filtered and dried the solid to give compound 52d (391.9 mg). MS m/z (M+H+) 273.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741887B2
Source datasetuspto-grants-2014_06
ORD IDord-901e22e0d9f641d085bcc34bac1ae3ec
Source noteuspto-grants-2014_06