HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693688Generated: November 1, 2026
Potassium Carbonate → (R)-3-(4-Fluorophenoxy)butanoic acid
https://huagongshe.com/reaction/1693688
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 7154394 | HCID 7154394 | — |
| Solvent | Water | HCID 962 | — |
| Product | (R)-3-(4-Fluorophenoxy)butanoic acid | HCID 57626400 | 184.5% |
Reaction Steps
6-fluoro-2,3-dihydro-2-methylchromen-4-oxime (13). To a suspension of the ketone 12 (2.79 g, 15.5 mmol) was added a solution of hydroxylamine hydrochloride (2.09 g, 30 mmol) and K2CO3 (1.2 g, 8.75 mmol) in 18 mL of H2O. The reaction mixture was refluxed for four hours. After cooling to room temperature, the solution was removed under vacuum, and the residual solid was triturated with ice water. The crude product was recrystallized from EtOH to give 3.2 g (84%) of the white solid oxime 13, m.p. 102-105° C., 1H NMR (CDCl3) δ 7.58 (br s, 1H), 7.48 (dd, J=3.0, 9.5 Hz, 1H), 6.97 (ddd, J=3.0, 9.0, 8.0 Hz, 1H), 6.85 (dd, J=4.5, 9.0 Hz, 1H), 4.21-4.15 (m, 1H), 3.28 (dd, J=3.0, 17.0 Hz, 1H), 2.37 (dd, J=12.0, 17.0 Hz, 1H), 1.47 (d, J=6.5 Hz, 3H). EI-MS (m/z) 195 (M+). The reaction is shown as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158667B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-6934df6784874f4da0216043c82093d2 |
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| Source note | uspto-grants-2012_04 |
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