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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055643Generated: October 29, 2026

Sodium Chloride → 3-(Morpholin-4-yl)-5-(pentafluoro-lambda6-sulphanyl)benzoic acid

https://huagongshe.com/reaction/1055643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantMorpholineHCID 8083—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 58137421HCID 58137421—
CatalystHCID 178439012HCID 178439012—
SolventTolueneHCID 1140—
Product3-(Morpholin-4-yl)-5-(pentafluoro-lambda6-sulphanyl)benzoic acidHCID 89699656—

Reaction Conditions

Temperature130 °C

Reaction Steps

1.5 g (4.6 mmol) of the compound of Example 15A and 0.48 g (5.5 mmol) of morpholine were dissolved in 15 ml of toluene, and the mixture was degassed with argon. 75 mg (0.09 mmol) of [2-(2-aminoethyl)phenyl](chloro)palladium-dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphane/tert-butyl methyl ether adduct, 44 mg (0.09 mmol) of dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphane and 1.06 g (11.0 mmol) of sodium tert-butoxide were added successively to this solution. The reaction was stirred in a microwave oven (Biotage Initiator, with Dynamic Field Tuning) at 130° C. for 30 min. The reaction was then stirred into 10 ml of saturated aqueous sodium chloride solution and extracted twice with in each case 30 ml of ethyl acetate. The organic phase was washed with pH 4 buffer solution, dried over sodium sulphate and concentrated on a rotary evaporator. The residue was dissolved in 5 ml of tert-butyl methyl ether, and 10 ml of pentane were added. The precipitate formed was filtered off and dried. This gave 1.04 g (68% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394309B2
Source datasetuspto-grants-2016_07
ORD IDord-4f25ee6e347d414db81215b1bf4f5ac4
Source noteuspto-grants-2016_07