HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128972Generated: October 27, 2026
Hydrochloric Acid → 5-(2-Nitroethyl)-1H-indole
https://huagongshe.com/reaction/128972
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-(2-nitro-vinyl)-1H-indole | HCID 54465016 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-(2-Nitroethyl)-1H-indole | HCID 13109723 | 40.6% |
Reaction Steps
A solution of sodium borohydride (2.0 g) and 40% w/v aqu. NaOH was added dropwise to a solution of the the product from step (b) (1.9 g) in acetonitrile (55 ml) at 0° C. The pH was maintained at 3-6 by periodic additions of 2N aqu. HCl. The resulting solution was stirred at 0° C. for 2 hours, then diluted with water and extracted with DCM. The combined extracts were washed with brine, dried and evaporated in vacuo to give a yellow oil which was eluted through a silica column using chloroform as eluant to give the desired product as a pale yellow oil (0.78 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05466699 |
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| Source dataset | uspto-grants-1995_11 |
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| ORD ID | ord-4a527876fe97424dabbbd777c642af79 |
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| Source note | uspto-grants-1995_11 |
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