HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930162Generated: November 2, 2026
Methanol → Methyl 2-(3,5-difluoro-4-hydroxyphenyl)propanoate
https://huagongshe.com/reaction/1930162
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 2-(3,5-Difluoro-4-methoxyphenyl)propanoic acid | HCID 59627718 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-(3,5-difluoro-4-hydroxyphenyl)propanoate | HCID 59627725 | 89% |
Reaction Steps
tribromoborane (7.37 mL, 77.99 mmol) was added dropwise to 2-(3,5-difluoro-4-methoxyphenyl)propanoic acid (Intermediate 21-4; 2.81 g, 13.00 mmol) in dichloromethane (96 mL) at 0° C. under nitrogen. The resulting solution was stirred at 0° C. for 1 hour. The reaction mixture was added dropwise to methanol (26.3 mL, 649.92 mmol) (—care reaction is vigorous and exothermic—MeOH kept in ice bath) and the mixture was stirred for a further 20 minutes. The reaction mixture was evaporated to dryness and redissolved in DCM (50 mL), and washed sequentially with saturated NaHCO3 (50 mL) and water (50 mL). The organic layer was dried with MgSO4 and evaporated to afford desired product methyl 2-(3,5-difluoro-4-hydroxyphenyl)propanoate (2.490 g, 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08188092B2 |
|---|
| Source dataset | uspto-grants-2012_05 |
|---|
| ORD ID | ord-dd340f11b4cc4ffc99bc1a98ac4f4d77 |
|---|
| Source note | uspto-grants-2012_05 |
|---|