HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909583Generated: October 30, 2026
Carbon Dioxide → 2,3-Difluoro-6-(2-methylallyloxy)benzoic acid
https://huagongshe.com/reaction/1909583
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,2-Difluoro-4-(2-methylallyloxy)benzene | HCID 58566701 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | 2,3-Difluoro-6-(2-methylallyloxy)benzoic acid | HCID 58566806 | — |
Reaction Steps
To a 1.4 M solution of sec-butyllithium in cyclohexane (6.7 mL) and anhydrous tetrahydrofuran (15 mL) at −75° C. was added 1,2-difluoro-4-(2-methylallyloxy)benzene (731) (1.6 g, 8.68 mmol). The resulting mixture was stirred at −75° C. for 2.5 hours and was then transferred to a round bottom flask containing dry ice. The resulting mixture was shaken for 5 min, and water (10 mL) was added dropwise. The mixture was acidified to pH 1 with concentrated hydrochloric acid and extracted with EtOAc (80 mL×3). The organic phase was washed with brine (60 mL×2), water (60 mL), and dried over anhydrous sodium sulfate, and the solvent removed in vacuo to give an oil 2,3-difluoro-6-(2-methylallyloxy)benzoic acid (732) (1.9 g), The product was used directly in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598374B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-80dc19bc2aa245779f8cb38270a68a92 |
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| Source note | uspto-grants-2013_12 |
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