HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 59596828, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 3-Fluorobenzyl chloride | HCID 9974 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl 3-hydroxyphenethylcarbamate | HCID 11031911 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59596828 | HCID 59596828 | 87.1% |
Reaction Steps
2.87 g (19.8 mmol) of 1-chloromethyl-3-fluoro-benzene in 5 ml of dry dimethylformamide were added to a suspension of 4.66 g (19.6 mmol) of [2-(3-hydroxy-phenyl)-ethyl]-carbamic acid tert-butyl ester, 4 g of K2CO3 and 0.3 g of potassium iodide in 50 ml of dry dimethylformamide. The reaction was first stirred at room temperature overnight, then was heated up to 50° C. for 6 hours. After evaporation of the solvent, water was added to the residue and the product was extracted with ethyl acetate. 7 g of crude oil were obtained. Purification by flash chromatography using a mixture of ethyl acetate/hexane (1:9→2:8 gradient) gave 5.9 g (86% yield) of the title product as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07855227B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-ab71620d230a4988915e4a34e0ab3a20 |
| Source note | uspto-grants-2010_12 |