HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401252Generated: October 25, 2026
Ammonium Chloride → 2-tert-Butyl-1H-indole
https://huagongshe.com/reaction/401252
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2,2,2'-Trimethylpropionanilide | HCID 2734005 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-tert-Butyl-1H-indole | HCID 594166 | 88% |
Reaction Steps
To a solution of 2,2-dimethyl-N-o-tolyl-propionamide (30.0 g, 159 mmol) in dry THF (100 mL) was added dropwise n-BuLi (2.5 M, in hexane, 190 mL) at 15° C. The mixture was stirred overnight at 15° C., cooled in an ice-water bath and treated with saturated NH4Cl solution. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were dried over anhydrous Na2SO4, filtered, and concentrated in vacuum. The residue was purified by column chromatography to give 2-tert-butyl-1H-indole (23.8 g, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741925B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-cbcef23d52a5486ca0f2d90ba47bfb92 |
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| Source note | uspto-grants-2014_06 |
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