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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092322Generated: October 31, 2026

Sodium borohydride → N-((4-bromo-5-methylthiophen-2-yl)methyl)-2,2-dimethoxyethanamine

https://huagongshe.com/reaction/2092322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178495904HCID 178495904—
SolventEthanolHCID 702—
ProductN-((4-bromo-5-methylthiophen-2-yl)methyl)-2,2-dimethoxyethanamineHCID 58466475—

Reaction Steps

(E)-N-((4-bromo-5-methylthiophen-2-yl)methylene)-2,2-dimethoxyethanamine (15.00 g, 51.34 mmol) was taken up in EtOH (50 ml) and treated with sodium borohydride (1.942 g, 51.34 mmol) slowly (some fizzing observed). The reaction was stirred at reflux for 3 hours and at room temperature overnight. The reaction was then concentrated under reduced pressure and the residue was taken up in a mixture of ethyl acetate and water. The layer were separated and the organic layer washed (2×) with an aqueous saturated solution of sodium bicarbonate, then with water and then brine. The organic layer was dried with sodium sulfate and concentrated under reduced pressure to give N-((4-bromo-5-methylthiophen-2-yl)methyl)-2,2-dimethoxyethanamine as a brown oil. MS (M+1) 295.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440674B2
Source datasetuspto-grants-2013_05
ORD IDord-4d64e0c6cc7d4f19aef41456212a5c87
Source noteuspto-grants-2013_05