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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410138Generated: October 25, 2026

Benzene → 1-O-Hexadecylglycerol

https://huagongshe.com/reaction/410138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantSolketalHCID 7528—
Reactant1-BromohexadecaneHCID 8213—
ReactantPotassium HydroxideHCID 14797—
SolventDiethyl EtherHCID 3283—
Product1-O-HexadecylglycerolHCID 72733—
Product2-Propanol, 1-(hexadecyloxy)-3-(triphenylmethoxy)-HCID 499613—

Reaction Steps

1-Hexadecyl-3-tritylglycerol was prepared as described in U.S. Pat. No. 6,838,452. In brief, D-acetone glycerol (4 grams), powdered potassium hydroxide (approximately 10 grams) and hexadecyl bromide (9.3 grams) in benzene (100 ml) were stirred and refluxed for 5 hours, while removing the water formed by azeotropic distillation (compare W. J. Baumann and H. K. Mangold, J. Org. Chem. 29: 3055, 1964 and F. Paltauf, Monatsh. 99:1277, 1968). The volume of the solvent was gradually reduced to about 20 ml, and the resulting mixture was cooled to room temperature and dissolved in ether (100 ml). The resulting solution was washed with water (2×50 ml), and the solvent was removed under reduced pressure. A 100 ml mixture of 90:10:5 methanol:water:concentrated hydrochloric acid was added to the residue and the mixture was refluxed for 10 minutes. The product was extracted with ether (200 ml) and was washed consecutively with water (50 ml), 10% sodium hydroxide (20 ml) and again with water (volumes of 20 ml) until neutral. The solvent was removed under reduced pressure and the product (8.8 grams) was crystallized from hexane to give 7.4 grams of pure 1-hexadecyl-glycerol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759557B2
Source datasetuspto-grants-2014_06
ORD IDord-864e0c432fa5446aad14f290a8f43ad1
Source noteuspto-grants-2014_06