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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979524Generated: November 1, 2026

Trifluoroacetic acid → HCID 13336230, compound

https://huagongshe.com/reaction/1979524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 13336188HCID 13336188—
SolventDichloromethaneHCID 6344—
ProductHCID 13336230HCID 1333623059.1%

Reaction Steps

To a solution of methyl 2-O-methyl-3-O-octadecyl-5-O-trityl-β-D-xylofuranoside (3.2 g) in dry methylene chloride (32 ml) was added trifluoroacetic acid (3.2 ml) in one portion at ambient temperature. After stirring for 1.5 hours at the same temperature, the yellow solution was washed with water, aqueous sodium bicarbonate and water succesively, dried, and evaporated under reduced pressure. The residue was triturated in n-hexane to remove triphenylcarbinol by filtration. The filtrate was evaporated and then the residue was purified by column chromatography on silica gel (40 g, elution by chloroform) to yield 1.21 g of methyl 2-O-methyl-3-O-octadecyl-β-D-xylofuranoside as a thick oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04481196
Source datasetuspto-grants-1984_11
ORD IDord-2f0a8d66337b4ba497182532ddd11643
Source noteuspto-grants-1984_11