HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930143Generated: November 1, 2026
Iodoethane → Methyl 2-(3-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)butanoate
https://huagongshe.com/reaction/1930143
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | Benzeneacetic acid, 3-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, methyl ester | HCID 58464478 | — |
| Catalyst | Silver | HCID 23954 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 2-(3-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)butanoate | HCID 59627654 | 62.9% |
Reaction Steps
Lithium bis(trimethylsilyl)amide (3.86 mL, 3.86 mmol) was added to methyl 2-(3-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate (Intermediate 2-7; 1 g, 3.22 mmol) in THF (10 mL) cooled to 0° C. under nitrogen. The resulting solution was stirred at 0° C. for 30 minutes. Iodoethane, stabilized with silver (0.258 mL, 3.22 mmol), was added and the reaction stirred for 30 minutes. Ammonium chloride (satd) (25 mL) added with vigorous stirring, ethyl acetate (50 mL) added and the organic phase separated, washed with water (25 mL) and saturated brine (25 mL). The organic layer was dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 10% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford methyl 2-(3-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)butanoate (0.686 g, 62.9%) as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188092B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-892af2e11a214dd999708109a5814543 |
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| Source note | uspto-grants-2012_05 |
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