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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877954Generated: October 30, 2026

Potassium Bromide → tert-Butyl 3,5-dideoxy-2,4-O-(1-methylethylidene)-L-erythro-hexuronate

https://huagongshe.com/reaction/877954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BromideHCID 253877—
Reactanttert-Butyl 2,4-dideoxy-3,5-O-(1-methylethylidene)-D-erythro-hexonateHCID 9816650—
ReactantSodium HypochloriteHCID 23665760—
Reactant(2-Azatricyclo[3.3.1.1~3,7~]decan-2-yl)oxidanylHCID 42643072—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 3,5-dideoxy-2,4-O-(1-methylethylidene)-L-erythro-hexuronateHCID 9881588—

Reaction Steps

To the −15° C. to −5° C. pre-cooled reaction mixture of AZADO (0.002 g), potassium bromide (0.22 g) and methylene chloride (30 ml) added 5 g of tert-butyl 2-((4R,6S)-6-(hydroxymethyl)-2,2-dimethyl-1,3-dioxan-4-yl)acetate. Stirred the reaction mixture for 15 minutes at −15° C. to −5° C. 19 ml of sodium hypochlorite solution was added to the reaction mixture at same temperature. Stirred the reaction mixture for 15 minutes. Quenched the reaction mixture with 10% aqueous sodium thiosulfate solution. 20 ml of water was added and separated the both aqueous and organic layers. Washed the organic layer with water followed by brine solution. Distilled off the solvent completely to get the title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987444B2
Source datasetuspto-grants-2015_03
ORD IDord-38cfc2d0ed21467189403a902cbdd5ae
Source noteuspto-grants-2015_03