HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745530Generated: October 26, 2026
Hydrochloric Acid → 2-(3-thienyl)benzaldehyde
https://huagongshe.com/reaction/745530
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | N,N-dimethyl-4-nitrosoaniline | HCID 8749 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-[2-(Bromomethyl)phenyl]thiophene | HCID 13552993 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(3-thienyl)benzaldehyde | HCID 4321315 | — |
Reaction Steps
To a solution of Compound 2b (1.98 mmol) in chloroform (5 mL) was added pyridine (9.88 mmol) and the reaction mixture heated at reflux for 1 hour under nitrogen. The solvent was removed in vacuo and the residue triturated with diethyl ether to give a white solid. The solid was dissolved in 95% aqueous ethanol (10 mL ) and N,N-dimethyl-4-nitrosoaniline (1.98 mmol) was added with stirring followed by the addition of sodium hydroxide (4.0 mmol) in water (3 mL). The reaction mixture was stirred for 16 hours at ambient temperature and then 6N hydrochloric acid (3 mL) was added. After 30 minutes, the solvent was removed in vacuo and the residue was diluted with water (10 mL) and extracted with diethyl ether (2×30 mL). The combined organic phases were washed with saturated aqueous sodium bicarbonate, brine and the solvent removed in vacuo to give crude Compound 2c as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04599341 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-c307eb18a9c64f08bbb10f86adf65512 |
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| Source note | uspto-grants-1986_07 |
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