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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567355Generated: October 29, 2026

Benzyl Bromide → 9-Benzyl-5-carbamoyl-4-methoxy-1-methylcarbazole

https://huagongshe.com/reaction/567355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 22738585HCID 22738585—
SolventDimethylformamideHCID 6228—
Product9-Benzyl-5-carbamoyl-4-methoxy-1-methylcarbazoleHCID 22739446—

Reaction Steps

A solution of 0.148 g of 5-carbamoyl-4-methoxy-1-methylcarbazole in 1.1 ml of dimethylformamide was added to 0.026 g of sodium hydride (60% in mineral oil) in 0.4 ml of dimethylformamide and stirred for 60 minutes at room temperature. Benzyl bromide (0.076 ml) was then added and the reaction was stirred overnight. The reaction mixture was poured into 20 ml of saturated ammonium chloride solution and then extracted twice with ethyl acetate. The extracts were washed with water and then with brine, dried over magnesium sulfate and concentrated. The residue was rinsed with hexane and dissolved in dichloromethane, filtered and concentrated to afford 0.21 g of the subtitle compound. FDMS m/e 344 (M+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177440B1
Source datasetuspto-grants-2001_01
ORD IDord-be730c92c0744fe99548a69368c35b5f
Source noteuspto-grants-2001_01