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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864527Generated: November 1, 2026

Sodium Hydroxide → 1-(4-Bromothiophen-2-yl)-N-methylmethanamine

https://huagongshe.com/reaction/1864527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-Bromothiophene-2-carbaldehydeHCID 87792—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantMethylamine hydrochlorideHCID 6364545—
SolventMethanolHCID 887—
Product1-(4-Bromothiophen-2-yl)-N-methylmethanamineHCID 4228203444%

Reaction Steps

18 g (260 mmol) of methylamine hydrochloride and then 7.5 g (100 mmol) of sodium cyanoborohydride are successively added to a solution of 10 g (50 mmol) of 4-bromo-2-thiophenecarboxaldehyde in 150 ml of methanol. The reaction medium is stirred at room temperature for 24 hours and then filtered under vacuum. After evaporating the filtrate to dryness, the residue is taken up in dichloromethane. The organic phase obtained is washed with 1N hydrochloric acid solution. The aqueous phase thus obtained is treated with aqueous 1N sodium hydroxide solution and extracted with dichloromethane. The organic phase is dried over magnesium sulfate, filtered and evaporated under vacuum. 4.5 g (44%) of (4-bromothiophen-2-ylmethyl)methylamine are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625914B2
Source datasetuspto-grants-2009_12
ORD IDord-98c5f74d1b2140fb908b636f0f2e9000
Source noteuspto-grants-2009_12