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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252671Generated: October 30, 2026

Imidazole → 1-Palmitoyl-3-t-butyldimethylsilyl-glycerol

https://huagongshe.com/reaction/252671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant1-MonopalmitinHCID 14900—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
SolventDichloromethaneHCID 6344—
Product1-Palmitoyl-3-t-butyldimethylsilyl-glycerolHCID 85395614100%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-palmitoyl-glycerol (33.0 g), dichloromethane (330 ml) and imidazole (13.6 g) were added into 1 L reactor, and the reaction mixture was cooled to 0° C. Then, t-butyl-dimethylsilylchloride (18.0 g) was added, and the reaction mixture was stirred for 2 hours. After filtering the reaction mixture, the solvent was removed by distillation under reduced pressure, and purified water (165 ml) and heptane (150 ml) were added for an extraction. The separated organic layer was extracted with purified water (80 ml) again, and then the organic layer was dehydrated with anhydrous MgSO4, and filtered. Then, the solvent was removed by distillation under reduced pressure to obtain 1-palmitoyl-3-t-butyldimethylsilyl-glycerol (yield: 100%) {1H NMR (400 MHz, CDCl3): δ 0.78-0.83 (m, 18H), 1.18-1.31 (m, 24H), 1.50-1.56 (m, 2H), 2.24 (t, 2H), 3.51-3.60 (m, 2H), 3.76-3.79 (p, 1H), 4.01-4.10 (m, 2H)}.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868196B2
Source datasetuspto-grants-2011_01
ORD IDord-20a7c72a83ef44bbb45614e8e4beb78a
Source noteuspto-grants-2011_01