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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681975Generated: October 26, 2026

3,4-dihydro-2H-pyran → benzyl (2S,3S,5R)-2-hexyl-3-[(t-butyldimethylsilyl)oxy]-5-[(tetrahydro-2H-pyran-2-yl)oxy]hexadecanoate

https://huagongshe.com/reaction/1681975

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-dihydro-2H-pyranHCID 8080—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactantbenzyl (2S,3S,5R)-2-hexyl-3-[(t-butyldimethylsilyl)oxy]-5-hydroxyhexadecanoateHCID 22847454—
SolventDichloromethaneHCID 6344—
Productbenzyl (2S,3S,5R)-2-hexyl-3-[(t-butyldimethylsilyl)oxy]-5-[(tetrahydro-2H-pyran-2-yl)oxy]hexadecanoateHCID 67935903—

Reaction Conditions

Temperature-15 °C

Reaction Steps

M)f) 350 mg of benzyl (2S,3S,5R)-2-hexyl-3-[(t-butyldimethylsilyl)oxy]-5-hydroxyhexadecanoate and 0.5 ml of freshly distilled 3,4-dihydro-2H-pyran were dissolved in 10 ml of methylene chloride and cooled to -15° C. A crystal of p-toluenesulfonic acid monohydrate was added thereto. The mixture was stirred until the reaction has finished. Thereupon, the solution was evaporated and the residue was chromatographed on silica gel. There were obtained 330 mg of benzyl (2S,3S,5R)-2-hexyl-3-[(t-butyldimethylsilyl)oxy]5-[(tetrahydro-2 H-pyran-2-yl)oxy]hexadecanoate, MS: 603 (M+ -t-butyl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05175186
Source datasetuspto-grants-1992_12
ORD IDord-b4cc2c6c7bd54aefae625584e9d8470f
Source noteuspto-grants-1992_12