HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922319Generated: November 1, 2026
Ethyl 2-(4-methoxyphenoxy)acetate → Ethyl 2-(4-hydroxyphenoxy)acetate
https://huagongshe.com/reaction/922319
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 2-(4-methoxyphenoxy)acetate | HCID 240125 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-(4-hydroxyphenoxy)acetate | HCID 13187337 | 20% |
Reaction Steps
To a 100 mL RB flask fitted with magnetic stirrer was charged 20 mL of DCM to the stirred solvent was added ethyl (4-methoxyphenoxy)acetate (2 g, 9.5 mmol) and Borontribromide (1.85 g, 11.0 mmol) was added at 0° C. Then it was stirred at 0° C. for 30-45 min. After completion of the reaction (reaction monitored by TLC), reaction mass quenched with Sodium bicarbonate and concentrated the reaction mixture and extracted with ethyl acetate. The organic layer was washed with brine and dried by anhydrous Na2SO4 and evaporated to dryness, the resulting crude compound was purified by column chromatography on silica gel using petroleum ether and ethyl acetate as eluent to give the product (0.2 g Yield: 20%): 1H NMR (300 MHz, DMSO-d6): δ 8.97 (s, 1H), 6.72-6.75 (d, 2H), 6.64-6.67 (d, 2H), 4.62 (s, 2H) 4.11-4.18 (q, 2H), 1.18-1.22 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278915B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-b684801ba30241f7bdfb915a38d5393c |
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| Source note | uspto-grants-2016_03 |
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