HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908533Generated: October 27, 2026
Water → 2-(5-nitro-1H-indol-2-yl)propan-1-ol
https://huagongshe.com/reaction/1908533
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | ethyl 2-(5-nitro-1H-indol-2-yl)propanoate | HCID 59129193 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(5-nitro-1H-indol-2-yl)propan-1-ol | HCID 59129392 | 83.6% |
Reaction Steps
To a cooled solution of LiAlH4 (1.0 M in THF, 1.2 mL, 1.2 mmol) in THF (5.3 mL) at 0° C. was added a solution of ethyl 2-(5-nitro-1H-indol-2-yl)propanoate (0.20 g, 0.76 mmol) in THF (3.66 mL) dropwise. After addition, the mixture was allowed to warm up to room temperature and was stirred at room temperature for 3 h. The mixture was cooled to 0° C. Water (2 mL) was slowly added followed by careful addition of 15% NaOH (2 mL) and water (4 mL). The mixture was stirred at room temperature for 0.5 h and was then filtered through a short plug of celite using ethyl acetate. The organic layer was separated from the aqueous layer, dried over Na2SO4, filtered and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (ethyl acetate/hexane=1/1) to give 2-(5-nitro-1H-indol-2-yl)propan-1-ol (0.14 g, 81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08598181B2 |
|---|
| Source dataset | uspto-grants-2013_12 |
|---|
| ORD ID | ord-4dcdf99be7b141d19d3bf30049531acc |
|---|
| Source note | uspto-grants-2013_12 |
|---|