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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091287Generated: November 1, 2026

Ammonium Chloride → 3-Methylthieno[2,3-c]pyridine-2-carbaldehyde

https://huagongshe.com/reaction/2091287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantCalcium ChlorideHCID 5284359—
ReactantEthyl 3-methylthieno[2,3-c]pyridine-2-carboxylateHCID 46941715—
CatalystHCID 178418406HCID 178418406—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product3-Methylthieno[2,3-c]pyridine-2-carbaldehydeHCID 8237429387%

Reaction Steps

To a mixture of ethyl 3-methylthieno[2,3-c]pyridine-2-carboxylate (2.00 g) synthesized above, calcium chloride (2.01 g), ethanol (30 mL) and tetrahydrofuran (30 mL) was added sodium borohydride (1.37 g) at 0° C., and the mixture was stirred at room temperature for 3 hr. Saturated aqueous ammonium chloride solution was added to quench the reaction, and the reaction mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure to give a pale-yellow solid. To a solution (40 mL) of the obtained solid in tetrahydrofuran was added active manganese dioxide (8.10 g), and the mixture was stirred at 50° C. for 8 hr. Manganese dioxide was filtered off, and the filtrate was concentrated under reduced pressure to give the title object compound (1.39 g, 87%) as a pale-brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-f86f14584d3843058d9f26a7087c7c4e
Source noteuspto-grants-2013_05