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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057609Generated: November 4, 2026

Benzyl Bromide → HCID 18671682, compound

https://huagongshe.com/reaction/1057609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPentaneHCID 8003—
ReactantSodium hydrideHCID 24758—
Reactant8-Fluoro-1,2,3,9-tetrahydro-4H-carbazol-4-oneHCID 22147745—
SolventDimethylformamideHCID 6228—
ProductHCID 18671682HCID 1867168270%

Reaction Steps

8-Fluoro-1,2,3,9-tetrahydro-4H-carbazol-4-one (2.23 g, 0.011 mol) is added to a slurry of pentane-washed NaH (0.59 g, 0.015 mol) in DMF (18 mL) and after stirring for 20 min, benzyl bromide (1.7 mL, 0.014 mol) is added. The mixture is stirred for 1 h at which time the mixture is partitioned between water and ethyl acetate. The combined organic layers are dried over sodium sulfate and concentrated to dryness. The resulting residue is chromatographed on silica gel (200 mL) using methanol/dichloromethane (1/99). The solids are then recrstallized from ethyl acetate/dichloromethane/hexane to give 2.25 g (70%) of the title compound; mp 183-184° C.; MS (ESI−) for C19H16FNO m/z 292.1 (M−H)−; IR (drift) 1639, 1631, 1495, 1459, 1434, 1359, 1246, 1219, 1193, 1125, 798, 789, 736, 730, 698 cm−1; 1H NMR (CDCl3) δ2.23, 2.58, 2.87, 5.51, 6.92, 7.03, 7.16, 7.29, 8.07. Anal. Calcd for C19H16FNO: C, 77.80; H, 5.50; N, 4.78. Found: C, 77.58; H, 5.59; N, 4.79.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06514968B1
Source datasetuspto-grants-2003_02
ORD IDord-1c81415ec12a4c8681716179b14c6885
Source noteuspto-grants-2003_02