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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501899Generated: November 1, 2026

Water → (S)-3-(Hexadecyloxy)propane-1,2-diol

https://huagongshe.com/reaction/1501899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-BromohexadecaneHCID 8213—
ReactantPotassium HydroxideHCID 14797—
Reactant(R)-SolketalHCID 736056—
SolventBenzeneHCID 241—
Product(S)-3-(Hexadecyloxy)propane-1,2-diolHCID 1044848773%

Reaction Steps

40 grams of (R)-(−)-2,2-dimethyl-1,3-dioxolane-4-methanol, 80 grams of powdered potassium hydroxide and 100 grams of hexadecyl bromide were stirred in 350 ml benzene and refluxed for 7 hours, while removing the water formed by azeotropic distillation. The volume of the solvent was gradually reduced to about 50 ml. The reaction mixture was cooled to room temperature, 300 ml of ice-cooled water was added, and the mixture was extracted 4 times with 150 ml dichloromethane. The combined organic phase was washed with water and the solvent was removed under reduced pressure. The obtained residue was dissolved in 500 ml of a 90:10:5 (v/v) mixture of methanol:water:concentrated hydrochloric acid, and the resulting solution was refluxed for 2 hours. After cooling to room temperature, 200 ml water was added. The product was extracted thrice with 200 ml chloroform, and washed consecutively with 200 ml water, 200 ml of a saturated aqueous sodium carbonate solution, and again with 200 ml water. The solvent was removed under reduced pressure and the product was crystallized from 450 ml petroleum ether at 4° C., yielding 69.93 grams of pure (S)-1-hexadecyl-sn-glycerol. The yield was 73%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206206B2
Source datasetuspto-grants-2015_12
ORD IDord-7e4bfca11710401ba9f646f466872d12
Source noteuspto-grants-2015_12