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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193851Generated: November 4, 2026

Iodoethane → HCID 59267483, compound

https://huagongshe.com/reaction/2193851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
Reactant5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indoleHCID 2734772—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59267483HCID 59267483—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° C. suspension of NaH (43 mg, 1.81 mmol) in THF (4 mL) was added a solution of 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole (400 mg, 1.65 mmol, Aldrich) in THF (4 mL). The reaction mixture was maintained at 0° C. for 15 min, iodoethane (0.200 mL, 2.47 mmol) was added and the reaction was heated, at 50° C. for 30 min. The mixture was partitioned between water and EtOAc. The aqueous layer was extracted with EtOAc and the combined organics were washed with brine, dried (Na2SO4), filtered, and concentrated. Chromatography over silica eluting with 1-8% EtOAc/hexanes afforded the title compound as a white solid. LC-MS: calculated for C16H22BNO2 271.16, observed m/e 273.2 (M+H)+ (Rt 2.09 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329914B2
Source datasetuspto-grants-2012_12
ORD IDord-546b14d28ac2426097cd9a361ff7e82a
Source noteuspto-grants-2012_12