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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055654Generated: November 1, 2026

Water → 3-Methyl-5-(pentafluorosulfur)benzoic acid

https://huagongshe.com/reaction/1055654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHexaneHCID 8058—
ReactantTrimethylaluminumHCID 16682925—
ReactantHCID 58137421HCID 58137421—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product3-Methyl-5-(pentafluorosulfur)benzoic acidHCID 66523589—

Reaction Conditions

Temperature150 °C

Reaction Steps

1.15 ml (2.29 mmol) of a 2 M solution of trimethylaluminium in a hexane fraction were added to a solution of 250 mg (0.764 mmol) of the compound of Example 15A and 27 mg (0.023 mmol) of tetrakis(triphenylphosphine)palladium(0) in 2.5 ml of anhydrous THF, and the mixture was then, under an argon atmosphere, heated in a microwave oven (Biotage Initiator, with Dynamic Field Tuning) at 150° C. for 120 min. After cooling to RT, about 10 ml of water were added, and the reaction mixture was extracted three times with in each case about 10 ml of ethyl acetate. The combined organic extracts were washed with saturated sodium chloride solution, dried over anhydrous magnesium sulphate, filtered and then concentrated to dryness on a rotary evaporator. The product was isolated by preparative HPLC (Method 9). Concentration of the product fractions and drying of the residue under high vacuum gave 98 mg (47% of theory, 95% pure) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394309B2
Source datasetuspto-grants-2016_07
ORD IDord-eb5b2df0583b4b52bcb99c30d943be22
Source noteuspto-grants-2016_07