HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283143Generated: November 1, 2026
Acetic Acid → 2-(2-Fluoro-4-methoxyphenyl)-2-propanol
https://huagongshe.com/reaction/2283143
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 2'-Fluoro-4'-methoxyacetophenone | HCID 592821 | — |
| Reactant | HCID 178418332 | HCID 178418332 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-Fluoro-4-methoxyphenyl)-2-propanol | HCID 13493844 | 98% |
Reaction Steps
A solution of 2-fluoro-4-methoxyacetophenone (78.1 g, 460 mmol) in tetrahydrofuran (58.6 ml) was added to 3M methylmagnesium chloride solution in THF (199 ml, 598 mmol) at 20 to 35° C. under a nitrogen atmosphere over 30 min without cooling. Additional THF (19.53 ml) was used to rinse all starting material into the vessel. After complete addition, the mixture was stirred at 30° C. for 10 min., then was quenched into acetic acid (52.6 ml, 920 mmol) and water (273 ml) at 5-25° C. THF (20 ml) was used to rinse the vessel. Heptane (156 ml) was then added. The biphasic mixture was stirred at 20-25° C. for 30 min, and then the organic layer was separated. The organic layer was assayed and was found to contain 83.0 g of the desired product, which corresponds to 98% yield. The organic layer was concentrated under vacuum to remove THF, then was flushed with IPAC (200 ml), and the volume was increased to 500 ml by addition of more IPAC. This was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145348B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-8be700fa6cb54655acc79d02c0cc0bb2 |
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| Source note | uspto-grants-2015_09 |
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