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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 178495904 | HCID 178495904 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-((4-bromo-5-methylthiophen-2-yl)methyl)-2,2-dimethoxyethanamine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08440674B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-4d64e0c6cc7d4f19aef41456212a5c87 |
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| Source note | uspto-grants-2013_05 |
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