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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267473Generated: November 1, 2026

2-Thiophenecarboxaldehyde → 1-(Thiophen-2-ylmethyl)piperidine

https://huagongshe.com/reaction/2267473

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ThiophenecarboxaldehydeHCID 7364—
ReactantPiperidineHCID 8082—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventDichloromethaneHCID 6344—
Solvent1,1-DichloroethaneHCID 6365—
SolventSodium BicarbonateHCID 516892—
Product1-(Thiophen-2-ylmethyl)piperidineHCID 14026221—

Reaction Steps

2-Thiophenecarboxaldehyde (1 g, 8.9 mmol) was dissolved in dichloroethane and treated with piperidine and sodium triacetoxyborohydride. The reaction was stirred at room temperature overnight. The reaction was diluted with dichloromethane and aqueous saturated sodium bicarbonate. The organic layer was separated out, washed with water and brine and dried with sodium sulfate. The volatile were removed in vacuo and the residue was purified by column chromatography on silica gel using a gradient of 2 to 8% of methanol in dichloromethane to obtain a brown oil. Yield=1.5 g. MS (M+H)+ 182.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858785B2
Source datasetuspto-grants-2010_12
ORD IDord-82391d9c14f748ea82522ad0db861645
Source noteuspto-grants-2010_12