HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633590Generated: October 26, 2026
Hydrochloric Acid → 4-tert-Butyl-1-fluoro-2-nitrobenzene
https://huagongshe.com/reaction/1633590
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Tert-Butylaniline | HCID 69861 | — |
| Reactant | Sodium Tetrafluoroborate | HCID 4343483 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-tert-Butyl-1-fluoro-2-nitrobenzene | HCID 22741893 | — |
Reaction Steps
To a cold (5° C.) suspension of 4-t-butylaniline in a mixture of conc. hydrochloric acid (25 ml) and water (25 ml) was added a solution of sodium nitrite (7.6 g, 0.11 mol) in water (10 ml) keeping the temperature at 5-7° C. At the end of the addition, the mixture was stirred for additionally 15 min, whereafter a solution of sodium tetrafluoroborate (15.4 g, 0.14 mol) in water (30 ml) was added dropwise, maintaining the temperature at 5-8° C. After another 15 min at 5° C. the diazonium salt was filtered off, dried with suction and washed with diethyl ether (yield: 21 g). The diazonium salt was decomposed by gentle heating to 120° C. on an oil-bath. The product was distilled off and collected to yield if (11.2, 73.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06503925B1 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-8fdf5632d7804cda8240cb348294e6f1 |
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| Source note | uspto-grants-2003_01 |
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