HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782031Generated: October 26, 2026
Methanol → 2-(2-hydroxy-4-methoxyphenyl)-N-methylacetamide
https://huagongshe.com/reaction/1782031
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 2-(2,4-dimethoxyphenyl)-N-methylacetamide | HCID 8180193 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(2-hydroxy-4-methoxyphenyl)-N-methylacetamide | HCID 69017352 | — |
| Product | 2-(4-hydroxy-2-methoxyphenyl)-N-methylacetamide | HCID 69019532 | — |
Reaction Steps
To a solution of 2-(2,4-dimethoxyphenyl)-N-methylacetamide (445 mg, 2.12 mmol) in CH2Cl2 (10 mL) was slowly added 1M BBr3 solution in CH2Cl2 (6.4 mL, 6.4 mmol). After addition was completed, the reaction mixture was stirred at 0° C. for 2.5 h, methanol (2 mL) was added and after 15 min the volatiles were removed in vacuo. The residue was dissolved in ethyl acetate, washed successively with aqueous NaHCO3 and H2O. The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by silica gel flash chromatography (0-5% methanol in dichloromethane) to give the subtitled compound (16 mg) along with 2-(4-hydroxy-2-methoxyphenyl)-N-methylacetamide (30 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07498338B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-4df6b0a2d19445ef82ebb5c8053a5c34 |
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| Source note | uspto-grants-2009_03 |
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