Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820605Generated: November 2, 2026

Sodium prop-2-enolate → (2S,3S,4S,5R,6S)-3,4,5-Tris-(tert-butyl-dimethyl-silanyloxy)-6-(2-[1,3]dioxolan-2-yl-4-nitro-phenoxy)-tetrahydro-pyran-2-carboxylic acid

https://huagongshe.com/reaction/1820605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium prop-2-enolateHCID 23669913—
Reactant(2R,3S,4S,5R,6S)-3,4,5-tris-(tert-butyl-dimethyl-silanyloxy)-6-(2-[1,3]dioxolan-2-yl-4-nitro-phenoxy)-tetrahydro-pyran-2-carboxylic acid allyl esterHCID 68983558—
SolventAllyl AlcoholHCID 7858—
Product(2S,3S,4S,5R,6S)-3,4,5-Tris-(tert-butyl-dimethyl-silanyloxy)-6-(2-[1,3]dioxolan-2-yl-4-nitro-phenoxy)-tetrahydro-pyran-2-carboxylic acidHCID 68982700100.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

The solution of 5.64 g (7.58 mmol) of the compound, presented according to Example LE3d, in 150 ml of allyl alcohol is mixed with 9.1 ml of a 1 M solution of sodium allyl alcoholate in allyl alcohol, and it is stirred for 2.5 hours at 50° C. It is concentrated by evaporation, mixed with water, extracted several times with dichloromethane, the combined organic extracts are washed with saturated sodium chloride solution and dried on magnesium sulfate. The residue that is obtained after filtration and removal of the solvent is purified by chromatography on fine silica gel, and 1.78 g (2.44 mmol, 32%) of the title compound as well as 1.87 g (2.43 mmol, 32%) of (2R,3S,4S,5R,6S)-3,4,5-tris-(tert-butyl-dimethyl-silanyloxy)-6-(2-[1,3]dioxolan-2-yl-4-nitro-phenoxy)-tetrahydro-pyran-2-carboxylic acid allyl ester are isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605136B2
Source datasetuspto-grants-2009_10
ORD IDord-23b623758f31488d8f71058893e410fc
Source noteuspto-grants-2009_10