HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40131Generated: October 29, 2026
Stannous Chloride → 5-Methoxy-2-(3-methylbut-1-ynyl)aniline
https://huagongshe.com/reaction/40131
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-Methoxy-1-(3-methylbut-1-ynyl)-2-nitrobenzene | HCID 59762351 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Methoxy-2-(3-methylbut-1-ynyl)aniline | HCID 59762435 | — |
Reaction Steps
To a solution of 4-methoxy-1-(3-methylbut-1-ynyl)-2-nitrobenzene (Compound 134, 2.97 g, 13.6 mmol) in THF (45 ml) and EtOH (15 ml) at 0° C. was added SnCl2 (12.9 g, 68 mmol), followed by NaBH4 (3.1 g, 81.6 mmol) in three equal portions with one hour between each addition. The reaction was stirred at 0° C. for a total of 3.5 h and was quenched with aqueous ammonia, filtered through a pad of Celite, extracted with EtOAc (×3). The combined organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by chromatography on silica gel (0→20% EtOAc-hexanes) to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524917B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-f0b8297e7b1d477f80d15eb3746d594b |
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| Source note | uspto-grants-2013_09 |
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