879551-04-9

  • Product Name:(3R,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxyMethyl)-3-Methyl-dihydrofuran-2(3H)-one
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Product Details

Purity:99%

Best Price 879551-04-9 (3R,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxyMethyl)-3-Methyl-dihydrofuran-2(3H)-one In Medicine  

  • Molecular Formula:C6H9FO4
  • Molecular Weight:164.133
  • Melting Point:142-143 oC (ethyl acetate heptane )** 
  • Boiling Point:352.7±42.0 °C(Predicted) 
  • PKA:11.46±0.60(Predicted) 
  • PSA:66.76000 
  • Density:1.42±0.1 g/cm3 (20 oC 760 Torr), Calc.* 
  • LogP:-1.00680 

(3R,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxyMethyl)-3-Methyl-dihydrofuran-2(3H)-one(Cas 879551-04-9) Usage

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Uses

(3R,4R,5R)-3-Fluoro-4-hydroxy-5-(hydroxymethyl)-3-methyldihydrofuran-2(3H)-one can be used for synthetic preparation for asymmetric synthesis of dibenzoyl fluoro methyl-D-ribono-γ-lactone via asymmetric aldol condensation and enzymic hydrolysis from isopropylidene-D-glyceraldehyde and Et fluoropropionate.

 

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879551-04-9 Process route

(4S,5R)-ethyl-5-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-4-meth-yl-1,3,2-dioxathiolane-4-carboxylate 2,2-dioxide
879551-01-6

(4S,5R)-ethyl-5-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-4-meth-yl-1,3,2-dioxathiolane-4-carboxylate 2,2-dioxide

(3R,4R,5R)-3?fluoro?4?hydroxy?5?(hydroxymethyl)?3?methyltetrahydrofuran?2?one
879551-04-9

(3R,4R,5R)-3?fluoro?4?hydroxy?5?(hydroxymethyl)?3?methyltetrahydrofuran?2?one

Conditions
Conditions Yield
(4S,5R)-ethyl-5-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-4-meth-yl-1,3,2-dioxathiolane-4-carboxylate 2,2-dioxide; With triethylamine tris(hydrogen fluoride); In dichloromethane; at 90 ℃; for 3h;
With hydrogenchloride; barium(II) chloride; In dichloromethane; at 50 ℃; for 5h; Solvent; Temperature; Concentration;
89%
Multi-step reaction with 2 steps
1.1: tetraethylammonium fluoride / 1,4-dioxane / 16 h / 120 °C
1.2: 3 h / 20 °C
2.1: water; hydrogenchloride / ethanol / 48 h / 20 °C
With hydrogenchloride; water; tetraethylammonium fluoride; In 1,4-dioxane; ethanol;
 
Multi-step reaction with 2 steps
1.1: triethylamine tris(hydrogen fluoride) / 2 h / 82 - 85 °C
2.1: hydrogenchloride / 0.5 h / 90 - 92 °C
2.2: 4 h
With hydrogenchloride; triethylamine tris(hydrogen fluoride);
 
Multi-step reaction with 2 steps
1: tetraethylammonium fluoride / 1,4-dioxane / 16 h / 120 °C
2: hydrogenchloride / ethanol; water / 48 h / 20 °C
With hydrogenchloride; tetraethylammonium fluoride; In 1,4-dioxane; ethanol; water;
 
(2R,3R,4R)-2-fluoro-4,5-O-isopropylidene-2-methyl-3-sulfooxy-3,4,5-thydroxypentanoic acid ethyl ester tetrabutylammoniun salt

(2R,3R,4R)-2-fluoro-4,5-O-isopropylidene-2-methyl-3-sulfooxy-3,4,5-thydroxypentanoic acid ethyl ester tetrabutylammoniun salt

(3R,4R,5R)-3?fluoro?4?hydroxy?5?(hydroxymethyl)?3?methyltetrahydrofuran?2?one
879551-04-9

(3R,4R,5R)-3?fluoro?4?hydroxy?5?(hydroxymethyl)?3?methyltetrahydrofuran?2?one

Conditions
Conditions Yield
With trifluoroacetic acid; In water; acetonitrile; at 80 ℃; for 1.5h;
100%

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