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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960122Generated: October 30, 2026

Iodoethane → HCID 59267483, compound

https://huagongshe.com/reaction/1960122

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 numberUS08410284B2
Source datasetuspto-grants-2013_04
ORD IDord-721c6b71e2b64eadbacdb1492c011fca
Source noteuspto-grants-2013_04