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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743352Generated: October 30, 2026

Benzyl Bromide → HCID 9967388, compound

https://huagongshe.com/reaction/1743352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 9856210HCID 9856210—
SolventTetrahydrofuranHCID 8028—
ProductHCID 9967388HCID 9967388—

Reaction Steps

A solution of 3-(5-methoxycarbonyl-2-furyl)-1H-indazole (2.0 g, 8.3 mmol) and benzyl bromide (2.5 mL, 21.0 mmol) in THF (100 mL) was added dropwise via dropping funnel to a suspension of sodium hydride (60% dispersion in oil: 0.50 g, 12.5 mmol) in THF (200 mL). The resultant mixture was stirred at room temperature for 20 h. The mixture was poured onto brine and the layers separated. The aqueous layer was extracted three times with ether and then the combined organic material was washed with saturated aqueous NaHCO3 solution, dried (MgSO4) and concentrated under reduced pressure. The residue was chromatographed on silica (EtOAc:cyclohexane 1:4) and then the product was recrystallised (EtOAc/hexane) to give a yellow solid: mp 137–138° C.; MS (EI) M+ 332; 1H-NMR (CDCl3) 3.97 (s, 3H), 5.67 (s, 2H), 7.03 (d, 1H, J=3.7 Hz), 7.22–7.43 (m, 9H), 8.27 (d, 1H, J=8.1 Hz); Anal. (C20H16N2O3) C, calcd 72.28; found 71.92, H, calcd 4.85; found 4.75, N, calcd 8.43; found 8.39.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07009056B2
Source datasetuspto-grants-2006_03
ORD IDord-2d9d9d5043de456f94d31dd3b40fa97b
Source noteuspto-grants-2006_03