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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468667Generated: October 27, 2026

Benzene → 1-O-Hexadecylglycerol

https://huagongshe.com/reaction/1468667

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 numberUS09006217B2
Source datasetuspto-grants-2015_04
ORD IDord-c1de5395019a4d758650a10107744b48
Source noteuspto-grants-2015_04