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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234174Generated: October 25, 2026

Chloride → tert-Butyl 2,4-dideoxy-3,5-O-(1-methylethylidene)-D-erythro-hexonate

https://huagongshe.com/reaction/234174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactantchloride (4R-cis)-6-(chloromethyl)-2,2-dimethyl-1,3-dioxane-4-acetic acid, 1,1-dimethylethyl esterHCID 86747487—
CatalystTetrabutylammonium BenzoateHCID 10981353—
Producttert-Butyl 2,4-dideoxy-3,5-O-(1-methylethylidene)-D-erythro-hexonateHCID 9816650—

Reaction Conditions

Temperature100 °C

Reaction Steps

Solid tetrabutylammonium benzoate obtained as above (126.47 g, 0.348 mole) was added in one portion to a mechanically stirred solution of the chloride (4R-cis)-6-(chloromethyl)-2,2-dimethyl-1,3-dioxane-4-acetic acid, 1,1-dimethylethyl ester prepared as in step (d) of Example 1 above (32.3 g, 0.116 mole) in HPLC grade 1-methyl-2-pyrrolidinone (465 ml) under argon. The resulting solution was stirred at 100° C. (internal temperature). After 30 to 60 minutes the reaction mixture became homogeneous and brown in color. The progress of the reaction was followed by TLC and GC analysis (TLC: Rf =0.47 for the chloride starting material; Rf =0.35 for the title compound (silica gel, Ether: Hexane, 4:6, visualization by Ce (SO4 )2 spray). After 6.5 hours the reaction was completed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05594153
Source datasetuspto-grants-1997_01
ORD IDord-6dd940ca42dd45989204e25a34732a24
Source noteuspto-grants-1997_01