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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493863Generated: October 30, 2026

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

https://huagongshe.com/reaction/1493863

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 dissolved 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 thoroughly, 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 numberUS05025005
Source datasetuspto-grants-1991_06
ORD IDord-20cac1201ff846d9bb7df4bab31df42d
Source noteuspto-grants-1991_06