HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691979Generated: October 30, 2026
2-Fluoro-4-iodoaniline → HCID 178527793, compound
https://huagongshe.com/reaction/1691979
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Fluoro-4-iodoaniline | HCID 185694 | — |
| Reactant | Potassium ethylxanthate | HCID 2735045 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178527793 | HCID 178527793 | — |
Reaction Steps
A mixture of 2-fluoro-4-iodoaniline (24.19 g, 0.100 mole) and potassium ethylxanthogenate (35.27 g, 0.220 mole) in N,N-dimethylformamide (80 mL) was stirred at 95° C. for 5 hours. The reaction mixture was cooled to room temperature then diluted with water (150 mL) and 1 N aqueous HCl (200 mL). The mixture was stirred at room temperature overnight. The resulting precipitate was collected by filtration and rinsed with water. The solid was dried overnight at 85° C. in a vacuum oven to provide 6-iodobenzo[d]thiazole-2-thiol. 1H NMR (300 MHz, CD3OD) δ ppm 7.09 (d, J=8 Hz, 1H), 7.70 (dd, J=2, 8 Hz, 1H), 8.10 (d, J=2 Hz, 1H), 13.82 (Sbroad, 1H); MS (DCI/NH3) m/z 294 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153813B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-2f808d5a08f74ca19a33b558f8adac6d |
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| Source note | uspto-grants-2012_04 |
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