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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089609Generated: October 31, 2026

Benzyl Bromide → HCID 14484895, compound

https://huagongshe.com/reaction/1089609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 14484893HCID 14484893—
ReactantHCID 178418361HCID 178418361—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 14484895HCID 14484895—

Reaction Steps

Sodium hydride (60% dispersion in mineral oil, 0.678 g, 16.95 mmol) was washed with petroleum ether then suspended in dry tetrahydrofuran (15 mL) and cooled in an icebath. A solution of 6 (3.00 g, 15.4 mmol) in dry tetrahydrofuran (16 mL) was added dropwise to the sodium hydride suspension. When the hydrogen evolution had ceased, benzyl bromide (3.03 g, 17.7 mmol) was added dropwise and the mixture allowed to stir at room temperature overnight. The reaction was diluted with hexane (20 mL), filtered, and the filtrate concentrated. The residue was taken up in ether (50 mL), washed with 2N HCl and brine, dried (MgSO4) and concentrated to give 7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04966907
Source datasetuspto-grants-1990_10
ORD IDord-b0d2f50119994a2ba4e5811fe7684f58
Source noteuspto-grants-1990_10