HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723168Generated: November 3, 2026
Hydrochloric Acid → 2-(4-chlorophenyl)thiophene
https://huagongshe.com/reaction/1723168
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Chloroaniline | HCID 7812 | — |
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-(4-chlorophenyl)thiophene | HCID 11971655 | — |
Reaction Steps
4-Chloroaniline (4.0 g, 31.4 mmol) is added to 4 ml of acetic acid and heated until all solid is dissolved. The solution is cooled to 5° and 5.2 ml of conc. HCl is added, followed by the dropwise addition of sodium nitrite (2.16 g, 31.4 mmol) in 32 ml of water. After addition is complete, the mixture is stirred at 5° for 1 hour. Thiophene (2.64 g, 2.5 ml, 31.4 mmol) in 25 ml of carbon tetrachloride is added to the mixture, followed by the dropwise addition of 25% aq. NaOH (ca. 6.8 ml). After 1 hour, the mixture is poured into water and extracted with chloroform, and the combined extracts are washed with brine, dried and stripped of solvent. The black residue is distilled at ca. 120° 0.35 mm to give 2-(4-chlorophenyl)thiophene, a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04859699 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-08ab1c466ec447b88edc5f0d6288ee08 |
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| Source note | uspto-grants-1989_08 |
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