HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468154Generated: October 29, 2026
N-Fluorobenzenesulfonimide → 3-Fluoro-5-phenyl-benzo[b]thiophene-2-carboxylic acid
https://huagongshe.com/reaction/468154
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Fluorobenzenesulfonimide | HCID 588007 | — |
| Reactant | 5-Phenylbenzo[b]thiophene-2-carboxylic acid | HCID 59626071 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Fluoro-5-phenyl-benzo[b]thiophene-2-carboxylic acid | HCID 59625825 | 72.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08623858B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-75071dfaca744072ba005782f23832d7 |
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| Source note | uspto-grants-2014_01 |
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