HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774309Generated: November 1, 2026
Epichlorohydrin → 2,3-Epoxypropyl 4'-methoxyphenyl ether
https://huagongshe.com/reaction/1774309
Participants
| Role | Name | HCID | Charge |
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| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-Methoxyphenol | HCID 9015 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,3-Epoxypropyl 4'-methoxyphenyl ether | HCID 16646 | 48% |
Reaction Steps
A solution of NaOH (0.35 g) in 10 mL of water was added to a mixture of 4-methoxyphenol (1.10 g, 8.5 mmol) and epichlorohydrin (0.80 mL, 10.2 mmol). The mixture was heated at 100° C. for 3 h. After cooling, the mixture is taken up with AcOEt (50 mL). The organic phase was separated, washed with brine, dried over Na2SO4 and evaporated under reduced pressure. The crude residue was chromatographed (Petroleum ether/AcOEt, 4:1, as eluent) to afford pure compound in 48% yield. 1H NMR (CDCl3): δ 2.73-2.75 (m, 1H), 2.89 (app t, 1H), 3.31-3.36 (m, 1H), 3.76 (s, 3H), 3.88-3.93 (m, 1H), 4.14-4.20 (m, 1H), 6.81-6.88 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09260400B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-98209fcee20f450ebbffa7a691cbfab6 |
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| Source note | uspto-grants-2016_02 |
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