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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantBenzeneacetic acid, 3-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, methyl esterHCID 58464478—
CatalystSilverHCID 23954—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2-(3-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)butanoateHCID 5962765462.9%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188092B2
Source datasetuspto-grants-2012_05
ORD IDord-892af2e11a214dd999708109a5814543
Source noteuspto-grants-2012_05