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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362982Generated: November 1, 2026

1-Bromo-3-chloropropane → tert-butyl 1-(3-chloropropyl)-1H-indole-2-carboxylate

https://huagongshe.com/reaction/2362982

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantSodium hydrideHCID 24758—
ReactantBoc-indoleHCID 11458614—
Producttert-butyl 1-(3-chloropropyl)-1H-indole-2-carboxylateHCID 58046682104.7%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a cold solution of tert-butyl 1H-indole-2-carboxylate (1.15 g, 4.94 mmol, 1 equiv) in dimthylformamide sodium hydride (60% dispersion) (237 mg, 5.92 mmol, 1.2 equiv) was added and the reaction stirred until all the sodium hydride has been consumed. 1-bromo-3-chloropropane (1.46 ml, 14.88 mmol, 3 equiv) was added and the reaction stirred at 60° C. for 16 h. The reaction was partitioned between ethyl acetate and water. The organic layer was further washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The resulting residue was purifed using the Biotage flash chromatography system (SNAP, 50 g cartridge, Rf=0.5, gradient—5%-25% ethyl acetate in hexanes) to afford the title compound as an oil (1.52 g, quant); MS for C16H20ClNO2 m/z 293.12 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691836B2
Source datasetuspto-grants-2014_04
ORD IDord-d89d4709e3da4968bd5f97b99ffd0b23
Source noteuspto-grants-2014_04