HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203323Generated: October 31, 2026
Methyl 2-Bromo-5-chlorobenzoate → HCID 46856402, compound
https://huagongshe.com/reaction/2203323
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 2-Bromo-5-chlorobenzoate | HCID 280500 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | 4,4,4-Trifluorobutanoic acid | HCID 2777085 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 46856402 | HCID 46856402 | — |
Reaction Steps
A THF solution of sodium bis(trimethylsilyl)amide (1.0M, 194 mL, 194 mmol) was added dropwise to a −78° C. THF (400 mL) solution containing methyl 2-bromo-5-chlorobenzoate (16.10 g, 64.5 mmol) and 4,4,4-trifluorobutyric acid (9.17 g, 64.5 mmol). After stirring for 15 minutes at −78° C. the solution was warmed to 0° C. and stirred for an additional 2 hours. The reaction was quenched with an excess of aqueous 1N HCl (ca 400 mL) and stirred overnight at room temperature. The solution was concentrated to remove the majority of the THF. The solution was then diluted with EtOAc and washed with 1N NaHCO3 (twice) and brine. The organic phase was then dried over anhydrous sodium sulfate, filtered and concentrated. The residue was purified by silica gel chromatography using a hexanes/EtOAc gradient to give the indicated compound (solid). 1H NMR (500 MHz, CDCl3): δ 7.58 (d, J=8.4 Hz, 1H); 7.41 (d, J=2.5 Hz, 1H); 7.33 (dd, J=8.5, 2.5 Hz, 1H); 3.22 (t, J=7.8 Hz, 2H); 2.68-2.56 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365574B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-d5d1dc20aa974f8682ae9d291f9d24af |
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| Source note | uspto-grants-2016_06 |
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