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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508449Generated: October 30, 2026

Sodium hydride → (2S,3S,4R,5S,6R)-2-(Acetoxymethyl)-6-(((Z)-1-(3-bromophenyl)-3-ethoxy-3-oxoprop-1-en-2-yl)oxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate

https://huagongshe.com/reaction/1508449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantEthyl 3-(3-bromophenyl)-2-oxopropanoateHCID 18371018—
Reactant(2S,3S,4R,5S,6R)-2-(Acetoxymethyl)-6-(((Z)-3-ethoxy-1-(2-fluorophenyl)-3-oxoprop-1-en-2-yl)oxy)tetrahydro-2H-pyran-3,4,5-triyl triacetateHCID 66980300—
Reactant2,3,4,6 tetra-O-acetyl-alpha-D-glucose bromideHCID 86702362—
Product(2S,3S,4R,5S,6R)-2-(Acetoxymethyl)-6-(((Z)-1-(3-bromophenyl)-3-ethoxy-3-oxoprop-1-en-2-yl)oxy)tetrahydro-2H-pyran-3,4,5-triyl triacetateHCID 6698029124%

Reaction Steps

The title compound was prepared as described for C4 using Ethyl 3-(3-bromophenyl)-2-oxopropanoate B16 (100 mg, 0.369 mmol), sodium hydride (9.74 mg, 0.406 mmol) and 2,3,4,6 tetra-O-acetyl-α-D-glucose bromide (152 mg, 0.369 mmol). The resulting compound was isolated in the form of white solid in 24% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221860B2
Source datasetuspto-grants-2015_12
ORD IDord-ef87ea907dab428cb43d9d9866e967d2
Source noteuspto-grants-2015_12