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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721010Generated: November 2, 2026

Trimethylsilyl triflate → 1-allyl-1-deoxy-2,3,4-tri-O-benzyl-alpha-L-fucopyranose

https://huagongshe.com/reaction/1721010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl triflateHCID 65367—
ReactantAllyltrimethylsilaneHCID 69808—
Reactant(3S,4R,5R,6S)-3,4,5-Tris(benzyloxy)-6-methyltetrahydro-2H-pyran-2-olHCID 2734155—
SolventAcetonitrileHCID 6342—
Product1-allyl-1-deoxy-2,3,4-tri-O-benzyl-alpha-L-fucopyranoseHCID 1534481079%

Reaction Steps

To a solution of 2,3,4-tri-O-benzyl-L-fucopyranose (11a, 10.0 g) in acetonitrile (100 ml) at 0° C., allyltrimethylsilane (12 ml) was added followed by trimethylsilyltrifluoromethanesulfonate (14.5 ml). The solution was warmed to room temperature and was stirred for 14 hours at room temperature. The mixture was quenched with water (100 ml) in an ice-water bath. The acetonitrile was evaporated in vacuo and the mixture was extracted with ethyl acetate (3×100 ml). The combined organic extracts were washed with saturated sodium carbonate solution, followed by saturated sodium chloride solution, dried over sodium sulfate, filtered and concentrated. The crude mixture was eluted on a silica gel column (150 ml, hexane:ethyl acetate, 10:1) to provide 1-allyl-1-deoxy-2,3,4-tri-O-benzyl-α-L-fucopyranose (11b, 9.2 g, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05508387
Source datasetuspto-grants-1996_04
ORD IDord-7977dd6953534378beaf585df6c9a2f8
Source noteuspto-grants-1996_04