HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272266Generated: November 1, 2026
Acetic Acid → 4-Bromoacetyl-3-fluorophenylboronic acid
https://huagongshe.com/reaction/272266
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 4-Acetyl-3-fluorophenylboronic acid | HCID 12133027 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Bromoacetyl-3-fluorophenylboronic acid | HCID 12133028 | — |
Reaction Steps
An oven-dried, 500-milliliter, 3-necked, round-bottomed flask was charged with 5 grams (27.4 millimole) of 4-acetyl-3-fluorophenyl boronic acid and 25 milliliters of methanol under a nitrogen atmosphere. The solution was cooled to 0° C. using an ice bath. To this solution was added 0.2 milliliters (0.55 equivalents) of glacial acetic acid. In a 100 milliliters Erlenmeyer flask was taken 1.27 milliliters (3.95 grams, 24 millimole, 0.9 equivalents) of elemental bromine dissolved in 4 milliliters of cold methanol. The bromine solution was added dropwise to the above solution at 0° C. using an addition funnel. With the addition of Br2, the solution slowly turned light orange and finally to dark orange when addition was complete. After about 5-6 hours, the progress of the reaction was monitored by NMR. Depending on the progress of reaction, another 10-20 mole % of bromine was added after cooling the solution to 0° C. Total reaction time was approximately 24 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07456156B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-255b8c1c74f649df9bec9013a881b36c |
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| Source note | uspto-grants-2008_11 |
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