Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971864Generated: November 1, 2026

Methane → 6-Methyl-1-benzothiophene-2-carboxylic acid

https://huagongshe.com/reaction/1971864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantSodium HydroxideHCID 14798—
Reactant3-Chloro-6-methyl-1-benzothiophene-2-carboxylic acidHCID 815185—
ReactantAmmonium formateHCID 2723923—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product6-Methyl-1-benzothiophene-2-carboxylic acidHCID 1281385095%

Reaction Steps

A suspension of palladium on 5% wet charcoal (50% water) (1.065 g) and ammonium formate (2.52 g) in methanol (30 ml) is stirred for 20 minutes in an inert atmosphere; a solution of 2.52 g of ammonium formate in 5 ml of water and a solution consisting of 2.26 g of 3-chloro-6-methyl-benzo[b]thiophene-2-carboxylic acid (18), 70 ml of methanol and 10 ml of 1N NaOH is then added. The mixture is kept under reflux stirring in an inert atmosphere for 15 hours. 0.425 g of Pd/C (5% wet) is then added, and the reaction mixture is again maintained under reflux for 24 hours. The mixture is then cooled, diluted with methanol, filtered through a Celite bed, and the catalyst is washed with further methanol. The filtrate is then evaporated until dry at low pressure and the residue treated with 70 ml of 1N HCl and 250 ml of ethyl acetate. The organic phase is washed with brine (3×) and evaporated until dry, to obtain 1.82 g of compound (1) in the form of a white solid; HPLC purity=98.2%, yield=94.7%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431684B2
Source datasetuspto-grants-2013_04
ORD IDord-ffc24dbf162543568d131bb53edb9c74
Source noteuspto-grants-2013_04