HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741869Generated: October 25, 2026
Methanol → Methyl 2-(3-hydroxyphenoxy)phenylacetate
https://huagongshe.com/reaction/1741869
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl 2-(3-methoxyphenoxy)phenylacetate | HCID 14620154 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-(3-hydroxyphenoxy)phenylacetate | HCID 14620155 | 92.3% |
Reaction Steps
Boron tribromide (12.89 g, 0.051 mol) was dissolved in dichloromethane (50 ml) and cooled to 0°-5° C. A solution of methyl 2-(3-methoxyphenoxy)phenylacetate (7.0 g; 0,026 mol) in dichloromethane (80 ml) was added dropwise, with stirring over 1 hour. After stirring at 0°-5° C. for 20 minutes the mixture was added dropwise, with stirring to absolute methanol (100 ml) maintaining the temperature at 0°-5° C. The resulting solution was poured into water (250 ml) containing sodium bicarbonate (12 g), and the resulting mixture was extracted with ether (500 mls). The organic phase was washed with water (3×200 ml) and saturated brine (150 ml). After drying and filtration, evaporation of the ether solution gave methyl 2-(3-hydroxyphenoxy)phenylacetate (D) (6.12 g, 92.3% yield) as a brown gum. This material was suitable for use in subsequent steps without further purification. However, chromatography using mixtures of ether and hexane as eluant gave material of higher purity as a viscous golden oil which rapidly darkened on exposure to air.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05334748 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-1d6383ec4a74413994147ad4017d3b84 |
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| Source note | uspto-grants-1994_08 |
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