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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212142Generated: October 30, 2026

p-Xylyl bromide → HCID 21964305, compound

https://huagongshe.com/reaction/2212142

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Xylyl bromideHCID 7721—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 5-Bromoindole-2-carboxylateHCID 259091—
SolventDimethylformamideHCID 6228—
ProductHCID 21964305HCID 21964305—

Reaction Steps

NaH (60%, 3.88 g, 96.98 mmol) was added portionwise to a stirring solution of ethyl 5-bromo-1H-indole-2-Carboxylate (20.0 g, 74.6 mmol) in DMF (140 mL) at 0° C. under a nitrogen atmosphere over a period of 10 min. The mixture was then warmed to room temperature. After the reaction mixture was stirred at room temperature for one hour, 4-methylbenzyl bromide (14.2 g, 74.6 mmol) was added and the mixture was stirred at room temperature overnight. The reaction was quenched with aqueous ammonium chloride and diluted with water. The aqueous mixture was extracted with ethyl acetate. The organic extract was washed with water and brine, dried over anhydrous magnesium sulfate. This mixture was concentrated to give a semi-solid contained 0.8 mole equivalent DMF. Mass spectrum (ESI, [M+H]+) m/z 372. 1H NMR (400 MHz, DMSO-d6) δ 7.93 (d, 1H, J=7.94 Hz), 7.55 (d, 1H, J=9.01 Hz), 7.40 (dd, 1H, J=8.85 and 1.98 Hz), 7.32 (s, 1H), 7.04 (d, 2H, J=7.96 Hz), 6.90 (d, 2H, J=7.94 Hz), 5.79 (s, 2H), 4.28 (q, 2H), 2.20 (s, 3H), and 1.28 ppm (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101903B2
Source datasetuspto-grants-2006_09
ORD IDord-d255c02a742e4920b85803b7e010b081
Source noteuspto-grants-2006_09