HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289164Generated: October 30, 2026
Allyl bromide → 2-Allyl-3-(3-fluoro-phenyl)-pentanedioic acid 1-methyl ester
https://huagongshe.com/reaction/2289164
Participants
| Role | Name | HCID | Charge |
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| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 3-(3-Fluorophenyl)-5-methoxy-5-oxopentanoic acid | HCID 45358900 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Allyl-3-(3-fluoro-phenyl)-pentanedioic acid 1-methyl ester | HCID 54468642 | — |
Reaction Steps
To a cooled (-78° C.) solution of LDA (7.1 mL, 2.0 M, 14.2 mmol) in 50 mL THF was added a solution of 3-(3-fluoro-phenyl)-pentanedioic acid monomethyl ester (2-4) (1.58 g, 6.58 mmol) in 10 mL THF gradually. The mixture was stirred for 40 min, treated with allyl bromide (1.71 mL, 19.7 mmol) at -78° C. and stirred overnight while it was warmed to room temperature. It was then concentrated and diluted with 20 mL CH2Cl2 and 15 mL EtOH. To the resulting solution was added EDAC (1.88 g, 9.87 mmol) and DMAP (25 mg, 0.02 mmol). After stirring for 5 hr, the reaction was quenched with 20 mL 10% NaHCO3 and extracted with EtOAc (×3). The combined organic layers were washed with brine, dried (Na2SO4) and concentrated to provide 2-5 as an oil, which was further purified using flash silica chromatography (Hexane/EtOAc, 4:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06090944 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-890de63308e34afea63bde5429652563 |
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| Source note | uspto-grants-2000_07 |
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