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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701595Generated: October 25, 2026

Allyl bromide → 1,2-di-O-(n-hexadecyl)-3-allyl-glycerol

https://huagongshe.com/reaction/1701595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
Reactant2,3-Bis(hexadecyloxy)propan-1-olHCID 102548—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1,2-di-O-(n-hexadecyl)-3-allyl-glycerolHCID 2346610393%

Reaction Conditions

Temperature60 °C

Reaction Steps

Sodium hydride (1.78 g. of 50 wt. % dispersion in mineral oil, 37 mmoles) was added at 60° C. to a solution of 1,2-di-O-(n-hexadecyl)-glycerol (10 g., 18.5 mmoles) in N,N-dimethylformamide (100 ml.), and the resulting solution stirred for 20 minutes at 60° C. Allyl bromide (4.47 g., 37 mmoles) was then added dropwise and the resulting mixture stirred for 3 hours at 90° C., cooled, cautiosly diluted with water (200 ml.) to quench the reaction, and extracted with ether (3×150 ml.). The combined ether extract was washed with saturated aqueous sodium chloride solution, dried (MgSO4), filtered and evaporated in vacuo to an oil, which was purified by silica gel chromatography (elution with benzene) [10 g., 93% yield, oil, n.m.r. (CDCl3) δ 5.66-6.16 (m, 1, --OCH2CH=CH2), 5.25 (d of doublets, 2, --OCH2CH=CH2) and 4.03 (d, 2, --OCH2CH=CH2)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04193999
Source datasetuspto-grants-1980_03
ORD IDord-ab42812d146c4f84a092492634ec97f7
Source noteuspto-grants-1980_03