HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404888Generated: October 30, 2026
Water → 2-Bromo-5-(4-isopropoxyphenoxy)-1,3,4-thiadiazole
https://huagongshe.com/reaction/404888
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-((5-Bromo-1,3,4-thiadiazol-2-yl)oxy)phenol | HCID 66545107 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Bromo-5-(4-isopropoxyphenoxy)-1,3,4-thiadiazole | HCID 69437371 | 99.3% |
Reaction Steps
A solution of Example 24B (1.4 g, 5.11 mmol) in N,N-dimethyl formamide (20 mL) was treated with K2CO3 (1.06 g, 7.66 mmol) and 2-iodopropane (5.1 mL, 51.1 mmol) and the reaction mixture was sealed in a screw-top pressure vessel and heated at 85° C. for 2 hours. The reaction was cooled to 25° C., poured into water (200 mL), and extracted with diethyl ether (2×100 mL). The combined organic layers were washed with water (3×80 mL) and brine (80 mL), dried (Na2SO4), filtered and evaporated to provide 1.6 g of a light brown solid. The residue was purified by flash chromatography on silica gel eluting with a solvent gradient from 1% to 14% ethyl acetate in hexanes to provide 0.8 g (50%) of the title compound as a clear colorless oil. 1H NMR (300 MHz, DMSO-d6) δ ppm 7.37 (d, J=9.19 Hz, 2H) 7.01 (d, J=9.19 Hz, 2H) 4.63 (heptet, J=5.88 Hz, 1H) 1.27 (d, J=5.88 Hz, 6H); MS (ESI) m/z 316.9 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08748627B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-60548d79cb5c4d238a3dab5b9a7a9ab2 |
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| Source note | uspto-grants-2014_06 |
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