Hot selling 2-Deoxy-D-ribonic-1,4-lactone CAS 34371-14-7 with factory price Company profile Wuhan Fortuna Chemical Co.,Ltd established in 2006, is a big integrative chemical enterprise being engaged in Pharmaceutical & its intermediates, Foo
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inquiryProduct name: 2-Deoxy-D-Ribonolactone CAS No.: 34371-14-7 Molecule Formula:C5H8O4 Molecule Weight:132.11 Purity: 95.0% Package: 5kg/drum Description:White or off-white powder Manufacture Standards:Enterprise Standard TESTING ITEM
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inquiryAnsciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
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inquiryWe are committed to providing our customers with the best products and services at the most competitive prices.Appearance:white powder Storage:Room temperature with sealed well Package:according to the clients requirement Application:Use as primary a
2-DEOXY-D-RIBONIC ACID-1,4-LACTONEAppearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
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inquirygood quality, competitive price, thoughtful after sale serviceAppearance:white powder Storage:Keep it in dry,shady and cool place Package:250mg Application:Pharma;Industry;Agricultural;chemical reaserch Transportation:by express or by sea Port:Any po
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1-(2'-Deoxy-β-D-erythro-pentafuranosyl)-7-nitroindole
A
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
In methanol for 15h; Irradiation; | A 97% B 59% |
Decomposition; Irradiation; |
3,4-O-(R)-benzylidene-2-deoxy-D-erythro-ribono-1,5-lactone
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With trifluoroacetic acid In chloroform; water at 70℃; for 10h; | 96% |
With trifluoroacetic acid In chloroform Heating; |
3-O-benzyl-2-deoxy-D-ribonolactone
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In methanol at 20℃; for 24h; | 96% |
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With rhodium hydrido (PEt3)3 complex; 1-Phenylbut-1-en-3-one In N,N-dimethyl-formamide at 40℃; for 4h; | 93% |
With bromine In water at 20℃; for 24h; Sealed tube; | 76% |
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With bromine In water at 20℃; for 120h; Inert atmosphere; | 90% |
With bromine In water for 96h; Ambient temperature; | 86% |
With bromine In water at 20℃; for 120h; Sealed tube; | 75% |
3-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-3-trimethylsilanyloxy-propionic acid ethyl ester
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With trifluoroacetic acid In tetrahydrofuran | 90% |
2-Deoxy-D-ribose
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With bromine In water at 25℃; for 120h; | 88% |
With bromine In water at 20℃; for 120h; | 78% |
With bromine; potassium carbonate In water at 20℃; for 8h; | 70% |
With bromine In water at 20℃; for 120h; Sealed tube; | |
With bromine In water at 20℃; for 120h; Sealed tube; |
Ethyl (4''R)-(2,2-dimethyl-1,3-dioxolan-4-yl)-3-hydroxypropionate
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With water; trifluoroacetic acid | 87% |
(-)-(S)-3-((R)-2,2-dimethyl[1,3]dioxolan-4-yl)-3-hydroxypropanoic acid methyl ester
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With trifluoroacetic acid In water for 2h; Ambient temperature; | 83.1% |
With trifluoroacetic acid In water | |
With trifluoroacetic acid In water | |
With trifluoroacetic acid In water for 2h; Ambient temperature; | |
With water; trifluoroacetic acid In tetrahydrofuran at 20℃; for 4h; |
3-O-p-Nitrophenyl-D-glucose
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With 3-ethyl-4,5-dimethylthiazol-3-ium bromide; potassium carbonate; benzalacetophenone In acetonitrile at 130℃; for 0.25h; Microwave irradiation; | 53% |
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With chloro-trimethyl-silane at 20℃; for 4h; | 26% |
2,3-O-isopropylidene-D-ribofuranose
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With 2-mesityl-2,5,6,7-tetrahydropyrrolo[2,1-c][1,2,4]triazolium chloride; 1,8-diazabicyclo[5.4.0]undec-7-ene In toluene at 50℃; for 16h; | 13% |
2'-Deoxyguanosine
A
2,4-diamino-6-hydroxy-5-formylaminopyrimidine
B
9-(2-deoxy-β-D-erythropentopyranosyl)-2,4-diamino-5-formamidopyrimid-6-one
C
9-(2-deoxy-α-D-erythropentopyranosyl)-2,4-diamino-5-formamidopyrimid-6-one
D
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With Nitrogen dioxide In water Irradiation; Further byproducts given; | A 2.8% B 3.1% C 7.9% D 2.1% |
2'-Deoxyguanosine
A
2-amino-1,9-dihydro-6H-purin-6-one
B
2,4-diamino-6-hydroxy-5-formylaminopyrimidine
C
(2S,3S,5R)-5-(2-amino-6-oxo-1H-purin-9(6H)-yl)-3-hydroxytetrahydrofuran-2-carbaldehyde
D
9-(2-deoxy-β-D-erythropentopyranosyl)-2,4-diamino-5-formamidopyrimid-6-one
E
9-(2-deoxy-α-D-erythropentopyranosyl)-2,4-diamino-5-formamidopyrimid-6-one
F
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With Nitrogen dioxide In water Mechanism; Irradiation; gamma radio lysis; | A n/a B 2.8% C 2.2% D 3.1% E 7.9% F 2.1% G n/a |
D-Glucose
L-Lysine hydrochloride
A
2-furanoic acid
B
5-hydroxymethyl-furan-2-carboxylic acid
F
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
In water for 30h; Product distribution; Heating; pH 4.5; |
2-Bromo-2-deoxy-D-arabinono-γ-lactone
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With hydrogen; triethylamine; palladium on activated charcoal In ethyl acetate Yield given; |
(S)-3-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-3-hydroxy-N,N-dimethyl-propionamide
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With trifluoroacetic acid In water 1) 90 deg C, 2 h 2) benzene, heating; Yield given; |
(S)-3-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-N,N-diethyl-3-hydroxy-propionamide
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With trifluoroacetic acid In water 1) 90 deg C, 2 h 2) benzene, heating; Yield given; |
(S)-3-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-N-methoxy-N-methyl-3-trimethylsilanyloxy-propionamide
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With trifluoroacetic acid for 2h; Heating; |
tert-butyl (4R)-4,5-O-isopropylidene-3,4,5-trihydroxypentanoate
A
(4R,5R)-4-hydroxy-5-hydroxymethyltetrahydrofuran-2-one
B
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With trifluoroacetic acid at 90 - 95℃; for 2h; Yield given. Yields of byproduct given. Title compound not separated from byproducts; |
3,5-O-Benzylidene-2-deoxy-D-ribonic Acid γ-Lactone
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
In chloroform; water; trifluoroacetic acid at 70℃; for 10h; |
methyl (3S,4R)-3-(tert-butyldimethylsiloxy)-4,5-(isopropylidenedioxy)pentanoate
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With trifluoroacetic acid for 3h; Ambient temperature; Yield given; |
2-deoxy-D-lyxonic acid
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
at 90℃; for 2h; Yield given; |
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With hydrogen; nickel; triethylamine In methanol for 3h; |
1-(2-deoxy-2-iodo-β-D-ribofuranosyl)uracil
A
2,2'-Anhydrouridine
B
(5S)-5-(hydroxymethyl)-5H-furan-2-one
F
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
In water-d2 for 4h; Product distribution; Mechanism; Irradiation; var. solvents, in the presence of O2, also <1'-D>-2'α-iodo-2'-deoxyuridine, other deoxyoligonucleotides; | A 2.0 % Spectr. B 2.0 % Spectr. C 1.0 % Spectr. D 4.0 % Spectr. E 13 % Spectr. F 1.0 % Spectr. |
1,6-anhydro-2,3-dideoxy-β-D-erythro-hexopyranos-2-ulose
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With hydrogenchloride; peracetic acid; dimethylsulfide; acetic acid Yield given. Multistep reaction; |
1-[(2S,4S,5R)-2-(2,2-Dimethyl-propionyl)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-1H-pyrimidine-2,4-dione
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With air; water for 6h; Ambient temperature; Irradiation; |
2'-Deoxyguanosine
B
9-(2-deoxy-α-D-erythro-pentofuranosyl)-1,9-dihydro-6H-purin-6-one
C
2-amino-1,9-dihydro-6H-purin-6-one
D
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
at 20℃; Decomposition; Radiolysis; Further byproducts given; |
2'-deoxyuridin-1'-yl radical
A
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With tetranitromethane; oxygen In water at 20℃; Rate constant; |
2'-Deoxycytidine
A
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With menadione; water; oxygen at 10℃; Irradiation; Further byproducts given; | A 9 mg B 8 mg C 6 mg D 2 mg |
tert-butyldimethylsilyl nitrate
2-deoxy-D-ribonolactone
3,5-di-O-(tert-butyldimethylsilyl)-2-deoxy-D-ribono-1,4-lactone
Conditions | Yield |
---|---|
With pyridine In tetrahydrofuran for 8h; | 99% |
triisopropylsilyl chloride
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With 1H-imidazole; dmap In acetonitrile at 20℃; | 98% |
With 1H-imidazole; dmap In ethyl acetate; toluene; acetonitrile | 98% |
With 1H-imidazole In N,N-dimethyl-formamide at 0 - 40℃; for 41h; | 94% |
tert-butyldimethylsilyl chloride
2-deoxy-D-ribonolactone
3,5-di-O-(tert-butyldimethylsilyl)-2-deoxy-D-ribono-1,4-lactone
Conditions | Yield |
---|---|
With 1H-imidazole In dichloromethane Ambient temperature; | 97.8% |
With 1H-imidazole; dmap In N,N-dimethyl-formamide at 20℃; for 18h; Inert atmosphere; | 96% |
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 24h; Inert atmosphere; | 80% |
Conditions | Yield |
---|---|
With chloro-trimethyl-silane; zinc In tetrahydrofuran at 20℃; for 4h; Barbier Coupling Reaction; | 86% |
tert-butylchlorodiphenylsilane
2-deoxy-D-ribonolactone
2-deoxy-3,5-di-O-(tert-butyldiphenylsilyl)-D-ribonolactone
Conditions | Yield |
---|---|
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 24h; Inert atmosphere; | 85% |
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 24h; | 83% |
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 24h; | 83% |
With 1H-imidazole In N,N-dimethyl-formamide for 18h; Ambient temperature; | |
With 1H-imidazole In N,N-dimethyl-formamide for 12h; |
2-deoxy-D-ribonolactone
2-Deoxy-D-ribitol
Conditions | Yield |
---|---|
With hydrogen; Rh/C In water at 130℃; under 60006 Torr; | 85% |
trityl chloride
2-deoxy-D-ribonolactone
5-O-trityl-2-deoxy-D-erythro-pentono-1,5-lactone
Conditions | Yield |
---|---|
In pyridine for 4h; Ambient temperature; | 84% |
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With bis-(1,2-dimethylpropyl)borane for 24h; Ambient temperature; | 79% |
With bis-(1,2-dimethylpropyl)borane In tetrahydrofuran for 22h; Ambient temperature; | |
With bis-(1,2-dimethylpropyl)borane In tetrahydrofuran | |
With sodium tetrahydroborate In acetic acid Yield given; | |
Multi-step reaction with 3 steps 1: imidazole / dimethylformamide / 3 h / Ambient temperature 2: 90.4 percent / DIBAL / toluene / 0.25 h / -78 °C 3: 62 percent / AcOH / tetrahydrofuran; H2O / 24 h / 60 - 70 °C View Scheme |
tetradecanoyl chloride
2-deoxy-D-ribonolactone
5-O-tetradecanoyl-2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With pyridine for 12h; Ambient temperature; | 78% |
tert-butylchlorodiphenylsilane
2-deoxy-D-ribonolactone
(4S,5R)-5-(((tert-butyldiphenylsilyl)oxy)methyl)-4-hydroxydihydrofuran-2(3H)-one
Conditions | Yield |
---|---|
With pyridine for 12h; Ambient temperature; | 78% |
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 16h; chemoselective reaction; | 5.1 g |
4,4'-dimethoxytrityl chloride
2-deoxy-D-ribonolactone
5'-O-(4,4'-dimethoxytrityl)-2'-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With pyridine at 20℃; for 4h; | 78% |
O-benzyl 2,2,2-trichloroacetimidate
2-deoxy-D-ribonolactone
3O,5O-dibenzyl-2-deoxy-1,4-ribonolactone
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid In 1,4-dioxane pH 3; | 74% |
1,3-Dichloro-1,1,3,3-tetraisopropyldisiloxane
2-deoxy-D-ribonolactone
(6aR,9aS)-2,2,4,4-tetraisopropyltetrahydro-8H-furo[3,2-f ][1,3,5,2,4]trioxadisilocin-8-one
Conditions | Yield |
---|---|
With 1H-imidazole In N,N-dimethyl-formamide at 25℃; Schlenk technique; Inert atmosphere; | 73% |
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 24h; | 72% |
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; Inert atmosphere; | 28% |
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 24h; | |
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 24h; | 2.42 g |
tert-butyldimethylsilyl chloride
2-deoxy-D-ribonolactone
5-tert-butyldimethylsilyl ether of (4S,5R)-4-hydroxy-5-hydroxymethyltetrahydrofuran-2-one
Conditions | Yield |
---|---|
With pyridine; silver nitrate In acetonitrile | 70% |
With 1H-imidazole In N,N-dimethyl-formamide; acetonitrile for 16h; | 65% |
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; Cooling with ice; | 58% |
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 8h; | 56.4% |
2-deoxy-D-ribonolactone
2,5-dideoxy-5-iodo-D-ribonic acid-γ-lactone
Conditions | Yield |
---|---|
With 1H-imidazole; carbon tetraiodide; triphenylphosphine In dichloromethane at 20℃; for 12h; Iodination; | 67% |
With 1H-imidazole; carbon tetraiodide; triphenylphosphine In dichloromethane |
p-toluenesulfonyl chloride
2-deoxy-D-ribonolactone
(2S,3R)-(3-hydroxy-5-oxotetrahydrofuran-2-yl)methyl 4-methylbenzenesulfonate
Conditions | Yield |
---|---|
In pyridine at -5℃; for 6h; | 57% |
Stage #1: 2-deoxy-D-ribonolactone With pyridine at -15℃; Stage #2: p-toluenesulfonyl chloride at -15 - 0℃; for 7h; | 54% |
acetic anhydride
2-deoxy-D-ribonolactone
(-)-(4S,5R)-4-acetoxy-5-acetoxymethyl-4,5-dihydrofuran-2(3H)-one
Conditions | Yield |
---|---|
With pyridine; dmap | 55% |
With 0,2,4-dichlorophenyl-0-methylisopropylamidothiophosphate In pyridine Ambient temperature; overnight; | |
With pyridine at 20℃; for 24h; Inert atmosphere; | 166 mg |
benzaldehyde
2-deoxy-D-ribonolactone
A
3,4-O-(R)-benzylidene-2-deoxy-D-erythro-ribono-1,5-lactone
Conditions | Yield |
---|---|
With hydrogenchloride for 20h; Ambient temperature; | A 52% B 8% |
With hydrogenchloride for 20h; Ambient temperature; | A 52% B 8% |
benzoyl chloride
2-deoxy-D-ribonolactone
Conditions | Yield |
---|---|
With pyridine | 43% |
acetone
2-deoxy-D-ribonolactone
3,4-O-isopropylidene-2-deoxy-D-ribono-1,5-lactone
Conditions | Yield |
---|---|
With hydrogenchloride for 20h; Ambient temperature; | 36% |
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