HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1525621Generated: October 28, 2026
Sodium Iodide → [4-(2-Hydroxyethoxy)phenyl](phenyl)methanone
https://huagongshe.com/reaction/1525621
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Ethylene carbonate | HCID 7303 | — |
| Reactant | 4-Hydroxybenzophenone | HCID 14347 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | [4-(2-Hydroxyethoxy)phenyl](phenyl)methanone | HCID 3090643 | — |
Reaction Steps
A mixture of ethylene carbonate (14.26 g), xylenes (1.19 g) and 4-hydroxybenzophenone (30.41 g) was heated to 88° C. Sodium iodide (1615 mg) was added. Heating was continued until the temperature of the mixture reached 169° C. The melt was cooled to 110° C. and methanol (12.76 g), sodium hydroxide (50% aqueous solution; 4.01 g), toluene (42.51 g) and water (28.88 g) were added. The lower layer was separated (‘cut’) and discarded. Toluene (18.1 g) was added and the solvents were evaporated by heating to the boiling point of 111° C. 4-(2-Hydroxyethoxy)benzophenone was isolated by crystallisation and filtration at 17° C. resulted in 34.1 g (92%) of beige crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09085519B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-6cac71288b8f430f9d3ca0f479b43ceb |
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| Source note | uspto-grants-2015_07 |
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