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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456523Generated: October 30, 2026

Sodium Chloride → HCID 58817759, compound

https://huagongshe.com/reaction/456523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantHexaneHCID 8058—
ReactantN-FluorobenzenesulfonimideHCID 588007—
ReactantHCID 58817714HCID 58817714—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58817759HCID 5881775982.7%

Reaction Conditions

Temperature-65 °C

Reaction Steps

At a temperature of −65° C. stir, under nitrogen, a solution of the 4-(2-bromo-6-fluoro-benzo[b]thiophen-3-yl)-piperazine-1-carboxylic acid tert-butyl ester (Example 28b) (15.59 g, 37.55 mmol) in anhydrous THF (247 mL) and add, dropwise, n-butyllithium in hexane (2.5M, 19.53 mL, 48.82 mmol). Stir for 30 min and then add, dropwise, N-fluorobenzenesulfonimide (17.76 g, 56.33 mmol) dissolved in anhydrous THF. Stir overnight at ambient temperature, cool the reaction to 0° C., add saturated NaCl solution and then water. Extract the mixture with EtOAc (3×'s), combine the extracts and wash with water and brine. Dry the extract (MgSO4), and concentrate to obtain 11.0 g of oil. Chromatograph the oil over silica gel (ether/pet. ether, 9:1) and obtain 6.28 g (52%) of red oil, MS, m/z, 354 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186724B2
Source datasetuspto-grants-2007_03
ORD IDord-6217a44ca8a747c7b19bd3e7efb2c004
Source noteuspto-grants-2007_03