HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489246Generated: October 29, 2026
Isopropyl iodide → HCID 60054823, compound
https://huagongshe.com/reaction/489246
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 60054739 | HCID 60054739 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 60054823 | HCID 60054823 | 67.9% |
Reaction Steps
A mixture of Example 67 (49.7 mg, 0.11 mmol), 2-iodo propane (26 μl, 0.26 mmol) and K2CO3 (36 mg, 0.26 mmol) was heated at 80° C. for 25 h in acetonitrile (2 ml). After cooling to room temperature, the insoluble salts were removed and the filtrate concentrated to dryness. The residue was partitioned between DCM/water. The organic layer was concentrated in vacuo and chromatographed over silica gel (eluent: DCM/MeOH 95/5) to yield the above-titled compound as an amorphous white solid (38.1 mg). 1H NMR (CDCl3): 9.21 (1H, s), 8.92 (2H, s), 7.56 (2H, d, J=8.0 Hz), 7.33 (2H, d, J=8.0 Hz), 7.20 (1H, m), 6.61 (2H, d, J=1.5 Hz), 3.90 (1H, dd, J1=12 Hz , J2=6 Hz), 3.4-3.5 (2H, m), 3.2-3.4 (1H, m), 3.28 (3H, s), 3.09 (1H, d, J=11 Hz), 2.79 (1H, m), 1.23 (6H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06977267B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-73815f33ac524782abbae9a6a3101070 |
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| Source note | uspto-grants-2005_12 |
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