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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701601Generated: October 26, 2026

Methanol → 1,2-di-O-(n-hexadecyl)-3-O-(3-formylbenzyl)-glycerol

https://huagongshe.com/reaction/1701601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHydrideHCID 166653—
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactant1,2-Di-O-(n-hexadecyl)-3-O-(3-cyanobenzyl)-glycerolHCID 23466158—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
Product1,2-di-O-(n-hexadecyl)-3-O-(3-formylbenzyl)-glycerolHCID 2346614840%

Reaction Steps

A solution of 1,2-di-O-(n-hexadecyl)-3-O-(3-cyanobenzyl)-glycerol (5.0 g., 7.6 mmoles) and diisobutylaluminum hydride (1.17 g., 8.2 mmoles) in benzene (25 ml.) was stirred for 16 hours at ambient temperature. The reaction mixture was treated with methanol (4.22 ml.) and water (2.5 ml.) and stirred to decompose unreacted hydride, and then filtered and extracted with benzene (3×25 ml.). The combined benzene extract was dried (Na2SO4), filtered and evaporated in vacuo to an oil, which was purified by silica gel chromatography (elution with benzene) [2.0 g., 40% yield, oil, ir (CHCl3) 1700 cm-1, n.m.r. (CDCl3) δ 10.1 (s, 1, --ArCHO)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04193999
Source datasetuspto-grants-1980_03
ORD IDord-a12694b864104a3d80e9346c7218e0a7
Source noteuspto-grants-1980_03