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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986912Generated: November 2, 2026

Sodium Chloride → HCID 58817759, compound

https://huagongshe.com/reaction/1986912

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 (3x'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 is 6.28 g (52%) of red oil, MS, m/z, 354 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550469B2
Source datasetuspto-grants-2009_06
ORD IDord-2ce30b0a11ee4b7f98d51b4abdc79fae
Source noteuspto-grants-2009_06