HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1990852Generated: October 25, 2026
Potassium Iodide → 3-(3-Ethoxy-5-hydroxymethyl-phenoxy)-2,2-dimethyl-propan-1-ol
https://huagongshe.com/reaction/1990852
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 3-Bromo-2,2-dimethyl-1-propanol | HCID 142501 | — |
| Reactant | 3-Ethoxy-5-(hydroxymethyl)phenol | HCID 59029682 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(3-Ethoxy-5-hydroxymethyl-phenoxy)-2,2-dimethyl-propan-1-ol | HCID 68699803 | — |
Reaction Steps
To a solution of 3-ethoxy-5-hydroxymethyl-phenol (0.3 g, 1.78 mmol, 1.0 equiv) in DMF (2 mL) was added cesium carbonate (2.32 g, 7.14 mmol, 4.0 equiv), potassium iodide (0.59 g, 3.57 mmol, 2.0 equiv) and 3-bromo-2,2-dimethyl-propan-1-ol (0.66 mL, 0.89 g, 5.35 mmol, 3.0 equiv) and the reaction mixture stirred under Ar at 100° C. for 24 h. The reaction mixture was filtered, the solid material washed with DMF and the organic filtrate evaporated to dryness under reduced pressure. The crude reaction mixture was suspended in water (20 mL), extracted with dichloromethane (3×50 mL), the combined organic phases washed with a sat. solution of sodium chloride (1×20 ml) and dried over Na2SO4 providing 0.15 g (33%) of the title compound in sufficient purity for the next reaction step. MS (ISP): 255.2 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07645753B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-33767aff2524486f90d9c666cc80d071 |
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| Source note | uspto-grants-2010_01 |
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