HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345228Generated: October 30, 2026
Potassium Iodide → HCID 70053829, compound
https://huagongshe.com/reaction/345228
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2,6-Dimethylphenol | HCID 11335 | — |
| Reactant | HCID 88127025 | HCID 88127025 | — |
| Product | HCID 70053829 | HCID 70053829 | 49% |
Reaction Steps
N-Benzyloxycarbonyl-L-phenylalanyl-L-alanine bromomethyl ketone (50 mg, 0.11 mmol) and 2,6-dimethylphenol (14 mg) were dissolved in dry DMF (5 mL) and blanketed with argon gas. The solution was treated with potassium iodide on alumina (80 mg, KF-alumina, 2:3) and stirred overnight at room temperature. Ethyl acetate was added and the inorganic salts were removed by filtration. The organic filtrate was washed with saturated NaCl solution (4×25 mL), then dried over anhydrous sodium sulfate. The solvent was evaporated and the residue was applied to a silica gel column. Then N-benzyloxycarbonyl-L-phenylalanyl-L-alanine 2,6-dimethylphenoxymethyl ketone was eluted with EtOAc/hexane (1:1) under pressure. Evaporation gave a white solid (30 mg, 49%), m.p. 167°-168° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05055451 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-85437cae12984cd791f67a0a03a8dc49 |
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| Source note | uspto-grants-1991_10 |
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