HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033823Generated: November 1, 2026
{[(2-Methyl-1-nitropropan-2-yl)sulfanyl]methyl}benzene → 2-Methyl-2-(benzylthio)propylamine
https://huagongshe.com/reaction/1033823
Participants
| Role | Name | HCID | Charge |
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| Reactant | {[(2-Methyl-1-nitropropan-2-yl)sulfanyl]methyl}benzene | HCID 14613816 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Methyl-2-(benzylthio)propylamine | HCID 423583 | 46% |
Reaction Steps
A solution of 2-benzylthio-1-nitro-2-methylpropane (19 g) in dry ether (75 cm3) was added dropwise over a period of about 1 h to a stirred suspension of lithium aluminium hydride (9.6 g) in dry ether (500 cm3), cooled in an ice bath. When the addition was complete the mixture was heated under reflux for an additional hour. Excess lithium aluminium hydride was destroyed by the careful addition of water, and then an aqueous solution of sodium potassium tartrate (500 cm3, 20% w/w) was added. The mixture was stirred until the solids had dissolved and the ether layer was then separated. The aqueous solution was then extracted with ether (3×50 cm3) and the combined extracts then dried (MgSO4). Removal of the ether under reduced pressure gave the crude product which was purified via recrystallisation of its hydrochloride salt from isopropanol. The purified amine (7.5 g, 46%) was obtained as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05312904 |
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| Source dataset | uspto-grants-1994_05 |
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| ORD ID | ord-93c31ce256744c6280bc9f304d831925 |
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| Source note | uspto-grants-1994_05 |
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