Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038414Generated: November 1, 2026

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

https://huagongshe.com/reaction/2038414

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 13c (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 13d (391.9 mg). MS m/z (M+H+) 273.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575363B2
Source datasetuspto-grants-2013_11
ORD IDord-d92dc0b7123e46c7b9c6ba46ac97af4b
Source noteuspto-grants-2013_11