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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507673Generated: November 3, 2026

2-Thiophenecarboxaldehyde → 2,2-Dimethoxy-N-(thiophen-2-ylmethyl)ethanamine

https://huagongshe.com/reaction/507673

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ThiophenecarboxaldehydeHCID 7364—
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product2,2-Dimethoxy-N-(thiophen-2-ylmethyl)ethanamineHCID 12337020—

Reaction Steps

Thiophene-2-carboxaldehyde (22.4g, 200 mmol) was dissolved in anhydrous ethanol (200 mL) and treated with 2,2-dimethoxyethanamine (26.6 g, 200 mmol) and para-toluenesulfonic acid hydrate (0.1 g, catalytic) and the mixture heated to reflux for 4 h. The reaction was allowed to cool down to room temperature and sodium borohydride (7.6 g, 200 mmol) was added in small portions to the reaction. Following complete addition, the reaction was stirred at room temperature for 15 min, then at reflux for 2 h. The reaction was allowed to cool down to room temperature and all the volatiles removed in vacuo. The residue was dissolved in ethyl acetate and was washed with saturated aqueous sodium bicarbonate, water and brine. The organic layer was then dried with sodium sulfate, passed through a pad of silica gel, concentrated and placed on a vacuum line to afford an off-white solid. Yield=40.1 g. MS (M+H)+ 202.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786132B2
Source datasetuspto-grants-2010_08
ORD IDord-4ce3156dd99e458480fc0e8403e0d2db
Source noteuspto-grants-2010_08