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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649049Generated: October 25, 2026

4-Toluenesulfonyl chloride → 3-O-Octadecyl-2-O-tosyl-1-O-tritylglycerol

https://huagongshe.com/reaction/649049

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant1-(Octadecyloxy)-3-(triphenylmethoxy)propan-2-olHCID 12896848—
SolventPyridineHCID 1049—
Product3-O-Octadecyl-2-O-tosyl-1-O-tritylglycerolHCID 1350652983.9%

Reaction Steps

In 9 ml of pyridine was dissoved 5.0 g (8.52 mmole) of 3-O-octadecyl-1-O-tritylglycerol, and after 1.95 g (10.22 mmole) of tosyl chloride was added to the solution, the mixture was stirred at room temperature overnight and concentrated to dryness under reduced pressure. The residue was dissolved in 50 ml of water and 50 ml of dichloromethane, and after shaking throroughly, the dichloromethane layer was separated out. The organic layer was concentrated to dryness under reduced pressure, and the residue was purified by silica gel column (50 g), with n-hexane.ethyl acetate (193:7) used as an eluent, to give 5.3 g (yield of 83.9%) of colorless needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04737518
Source datasetuspto-grants-1988_04
ORD IDord-b87711f4a21f4010912c3d0924dad1eb
Source noteuspto-grants-1988_04