HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270732Generated: October 25, 2026
Hydrochloric Acid → 4-Aminophenylsulphur pentafluoride
https://huagongshe.com/reaction/270732
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | 4-Nitrophenylsulfur Pentafluoride | HCID 2775740 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Aminophenylsulphur pentafluoride | HCID 2779190 | 99.3% |
Reaction Steps
A solution of tin(II) chloride (1465 g., 7.73 mol) in concentrated (32 percent) aqueous HCl solution was heated with stirring to 80° C. and then, with ice cooling, 4-nitrophenylsulfur pentafluoride (584 g., 2.344 mol) was introduced in 8 portions over the course of 1 h. The internal temperature was kept below 100° C. during this. Subsequently, the mixture was stirred at an internal temperature of 85° C. for 1.5 h and then cooled to 45° C. over the course of a further hour. A mixture of ice (12 kg), NaOH (2 kg) and dichloromethane (1.5 l) was prepared and added to the reaction mixture with vigorous stirring. The phases were separated, the aqueous phase was extracted 3 times with 1 l of dichloromethane each time, and the combined organic phases were dried over Na2SO4 and evaporated in vacuo. 510 g (99%) of 4-aminophenylsulfur pentafluoride were obtained as a pale yellow crystalline powder, m.p. 63-65° C. (Bowden, R. D., Comina, P. J., Greenhall, M. P., Kariuki, B. M., Loveday, A., Philip, D. Tetrahedron 2000, 56, 3399: 56-59° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07449594B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-706f09174b2e45949271e3387a724a43 |
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| Source note | uspto-grants-2008_11 |
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