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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410139Generated: October 28, 2026

Acetic Acid → HCID 25155178, compound

https://huagongshe.com/reaction/410139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 25155177HCID 25155177—
CatalystBetaine Hydrazide HydrochlorideHCID 67156—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductHCID 25155178HCID 2515517827%

Reaction Steps

As depicted in Scheme III, 1-Hexadecyl-2-(5′,6′-dihydroxy-hexanyl)-glycerol (7.84 grams) was dissolved in isopropanol (50 ml) and water (12 ml). NaIO4 (9 grams) was added and the reaction mixture was stirred at room temperature for 3 hours. Water (50 ml) was added and the reaction mixture extracted with chloroform (3×50 ml). dried over anhydrous Na2SO4, filtered and the solvent removed under to reduced pressure yielding 5.56 grams. The crude product was dissolved in ethanol (60 ml) and glacial acetic acid (2.3 grams). Girard's reagent T (5.6 grams) was added and the reaction mixture was refluxed for 2 hours. The reaction mixture was cooled in ice-bath, alkaline solution (2.3 grams in 45 ml water) was added and the mixture was extracted with ether (3×25 ml). The etheral phase was washed with water and the water combined with the alkaline phase. The aqueous phase was acidified with concentrated HCl (4.4 ml) and extracted with ether (3×25 ml). Washing with water, saturated aqueous sodium bicarbonate (3×25 ml), water (2×25 ml). drying over anhydrous Na2SO4 and removal of the solvent under reduced pressure gave 1.95 grams (0.0049 mol) of 1-Hexadecyl-2-(5′-oxo-pentanyl)-glycerol (26.9% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759557B2
Source datasetuspto-grants-2014_06
ORD IDord-b06865bbc1e04301a2228a0fa8e64a81
Source noteuspto-grants-2014_06