HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930106Generated: October 31, 2026
Methanol → Methyl 2-(2-chloro-2',6'-difluoro-4'-hydroxybiphenyl-4-yl)acetate
https://huagongshe.com/reaction/1930106
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 2-(2-Chloro-2',6'-difluoro-4'-methoxybiphenyl-4-yl)acetic acid | HCID 59627715 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-(2-chloro-2',6'-difluoro-4'-hydroxybiphenyl-4-yl)acetate | HCID 59627694 | 100% |
Reaction Steps
Boron tribromide (1.494 mL, 15.80 mmol) was added dropwise to 2-(2-chloro-2′,6′-difluoro-4′-methoxybiphenyl-4-yl)acetic acid (Intermediate 2-5; 822 mg, 2.63 mmol) in dichloromethane (30 mL) at ambient temperature under nitrogen. The resulting solution was stirred at ambient temperature for 90 minutes. The reaction mixture was cautiously added to ice water cooled methanol (50 mL) and the mixture was stirred for a further 20 minutes. The reaction mixture was evaporated to dryness and redissolved in EtOAc (150 mL), and washed sequentially with 2M HCl (50 mL) and saturated brine (50 mL). The organic layer was dried over MgSO4, filtered and evaporated to afford methyl 2-(2-chloro-2′,6′-difluoro-4′-hydroxybiphenyl-4-yl)acetate (822 mg, 100%) as a yellow gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188092B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-aa3013bcf67543ef97e805665623c991 |
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| Source note | uspto-grants-2012_05 |
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