HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742775Generated: October 25, 2026
Epichlorohydrin → 2-[(4-Benzoylphenoxy)methyl]oxirane
https://huagongshe.com/reaction/1742775
Participants
| Role | Name | HCID | Charge |
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| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | 4-Hydroxybenzophenone | HCID 14347 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Product | 2-[(4-Benzoylphenoxy)methyl]oxirane | HCID 352816 | 83% |
Reaction Steps
1 g of 4-hydroxy benzophenone and 4.668 g of epichlorohydrin (0.025 mol) were dissolved, 20.5 mg of sodium hydroxide was added, and the reaction system was heated to 100° C. and then cooled to 95° C. Furthermore 201.4 mg of sodium hydroxide was added, and additional heating and agitation was carried out for 3 hours. The system was cooled to the room temperature, and salt was removed by filtering. The obtained filtrate was condensed under reduced pressure condition, and purified according to the silica gel chromatography to obtain 1.0 g of solid state 4-glycidyloxy benzophenone (Yield: 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05342610 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-e85f38e65d7646519f71c006d78eed22 |
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| Source note | uspto-grants-1994_08 |
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