HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974374Generated: October 27, 2026
2-Nitropropane → 3-Bromo-7-benzothiophene-carbaldehyde
https://huagongshe.com/reaction/974374
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Nitropropane | HCID 398 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 3-Bromo-7-bromomethylbenzothiophene | HCID 14780522 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Bromo-7-benzothiophene-carbaldehyde | HCID 19986344 | — |
Reaction Steps
With stirring, 68.2 g (0.74 mole) of 2-nitropropane are added dropwise at room temperature, over a period of 45 minutes, to a Na-ethoxide solution prepared under an argon atmosphere from 14.2 g (0.61 mole) of sodium and 800 ml of abs. ethanol. 137 g (0.61 mole) of 3-bromo-7-bromomethylbenzothiophene are then added dropwise at room temperature, over a period of 1.5 hours, to the resulting white suspension. After the reaction mixture has been stirred for one day, the solvent is evaporated off from the reaction mixture in vacuo, the resulting residue of 101.2 g is dissolved in a mixture of hexane:diethyl ether 1:1 and the solution is purified by chromatography on silica gel. After evaporation of the solvent, 81 g (80% of the theoretical amount) of 3-bromo-7-benzothiophene-carbaldehyde are obtained as residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05068359 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-1ae22274ec364f248ee7d34599f174ce |
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| Source note | uspto-grants-1991_11 |
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