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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843512Generated: October 30, 2026

Benzyl Bromide → HCID 18427235, compound

https://huagongshe.com/reaction/843512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant1-BromooctadecaneHCID 8218—
ReactantSodium hydrideHCID 24758—
ReactantSerinolHCID 68294—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18427235HCID 18427235—

Reaction Steps

A solution of 2-amino-1,3-propanediol in THF is added dropwise with vigorous stirring to a suspension of sodium hydride over a period of 45 minutes to 2 hrs. The reaction mixture is stirred at room temperature for an additional hr and sequentially treated with a solution of one equivalent each of octadecyl bromide and benzyl bromide, respectively. The reaction mixture is stirred at room temperature for 4-14 hrs. The reaction mixture is worked up by extraction with methylene chloride. The methylene chloride layer is washed with water (3×50 mL), saturated NaCl (1×50 mL) and dried (MgSO4). The dried organic layer is evaporated under vacuum to afford the product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06379930B1
Source datasetuspto-grants-2002_04
ORD IDord-f012cdd77d3a4454b5da2b56b39c7d00
Source noteuspto-grants-2002_04