Conditions | Yield |
---|---|
stannous octoate; Nafion-H at 145℃; for 7h; Product distribution / selectivity; | 99.5% |
With sulfuric acid |
Conditions | Yield |
---|---|
With dichromic acid at 105 - 110℃; for 3h; Green chemistry; Large scale; | 99% |
With 3H(1+)*O40SiW12(4-)*C21H22O3PS(1+) Reflux; Dean-Stark; | 96.5% |
iodine for 20h; Heating; | 95% |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid at 120℃; under 760.051 Torr; for 12h; Time; | 98% |
for 6h; Dean-Stark; Reflux; | 46 %Chromat. |
With tin(II) oxide In 5,5-dimethyl-1,3-cyclohexadiene; water at 120℃; Reagent/catalyst; Dean-Stark; |
Conditions | Yield |
---|---|
Stage #1: LACTIC ACID With potassium carbonate In water at 20 - 90℃; for 1h; Stage #2: 1-bromo-butane at 20 - 40℃; for 8h; Reagent/catalyst; Temperature; | 97.5% |
LACTIC ACID
butan-1-ol
A
2-lactoyloxy-propionic acid butyl ester
B
n-butyl lactate
Conditions | Yield |
---|---|
aluminium(III) triflate In iso-tridecanol; di-isopropyl ether; water at 66 - 120℃; under 150.015 - 7500.75 Torr; for 6h; Conversion of starting material; | A 4% B 95% |
n-butyl lactate
Conditions | Yield |
---|---|
With dibromotriphenylphosphorane In dichloromethane at -50℃; for 3h; | 94% |
Conditions | Yield |
---|---|
With tin (IV) chloride pentahydrate at 110℃; for 6h; | 88.4% |
Conditions | Yield |
---|---|
aluminium(III) triflate at 120 - 140℃; under 37.5038 - 7500.75 Torr; for 1.5 - 6h; Conversion of starting material; | 70.9% |
zirconium(IV) triflate at 120 - 140℃; under 37.5038 - 7500.75 Torr; for 1 - 6h; Conversion of starting material; | 46.6% |
Conditions | Yield |
---|---|
Sn-BEA at 160℃; under 15001.5 Torr; Inert atmosphere of argon; | A 26% B 8% |
Sn-BEA at 160℃; for 20h; Inert atmosphere; autoclave; | A 26% B 8% |
LACTIC ACID
n-butyl lactate
Conditions | Yield |
---|---|
at 100 - 120℃; unter vermindertem Druck; man kocht 25 Stdn. mit Butylalkohol; |
Conditions | Yield |
---|---|
With 2-(diethylamine)ethanethiol | |
With titanium-silicon molecular sieve TS-1; tin-silicon molecular sieve Sn-Beta at 60℃; for 7h; |
Conditions | Yield |
---|---|
With sulfuric acid; benzene unter azeotropem Abdestillieren des Reaktionswassers; | |
With sulfuric acid; toluene unter azeotropem Abdestillieren des Reaktionswassers; |
Conditions | Yield |
---|---|
With sulfuric acid; benzene unter azeotropem Abdestillieren des Reaktionswassers; | |
With sulfuric acid; toluene unter azeotropem Abdestillieren des Reaktionswassers; |
Conditions | Yield |
---|---|
In diethyl ether Heating; |
Conditions | Yield |
---|---|
With water und Entfernen des entstehenden Wassers und Ammoniaks; |
Glyceraldehyde
butan-1-ol
A
1,1-dibutoxy-2-propanone
B
n-butyl lactate
Conditions | Yield |
---|---|
tin(IV) chloride at 90℃; for 1h; | A n/a B 82 % Chromat. |
2-oxopropanal
butan-1-ol
A
1,1-dibutoxy-2-propanone
B
n-butyl lactate
Conditions | Yield |
---|---|
tin(ll) chloride at 90℃; for 3h; | A n/a B 78 % Chromat. |
dihydroxyacetone
butan-1-ol
A
1,1-dibutoxy-2-propanone
B
n-butyl lactate
Conditions | Yield |
---|---|
tin(IV) chloride at 90℃; for 1h; | A n/a B 91 % Chromat. |
With Zeolite USY CBV 600 at 109.84℃; for 4h; Autoclave; | A 28 %Chromat. B 71 %Chromat. |
Conditions | Yield |
---|---|
aluminium(III) triflate at 125 - 145℃; under 37.5038 - 7500.75 Torr; Conversion of starting material; |
Conditions | Yield |
---|---|
In diethylene glycol dimethyl ether |
n-butyl pyruvate
n-butyl lactate
Conditions | Yield |
---|---|
With Streptomyces avermitilis α-keto ester reductase I, Mr 71.6 kDa by gel filtration; NAD at 37℃; for 6h; aq. phosphate buffer; |
Conditions | Yield |
---|---|
for 24h; |
Conditions | Yield |
---|---|
stannous octoate; Nafion-H at 145℃; for 7h; Product distribution / selectivity; | 99.5% |
With sulfuric acid |
Conditions | Yield |
---|---|
With dichromic acid at 105 - 110℃; for 3h; Green chemistry; Large scale; | 99% |
With 3H(1+)*O40SiW12(4-)*C21H22O3PS(1+) Reflux; Dean-Stark; | 96.5% |
iodine for 20h; Heating; | 95% |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid at 120℃; under 760.051 Torr; for 12h; Time; | 98% |
for 6h; Dean-Stark; Reflux; | 46 %Chromat. |
With tin(II) oxide In 5,5-dimethyl-1,3-cyclohexadiene; water at 120℃; Reagent/catalyst; Dean-Stark; |
Conditions | Yield |
---|---|
Stage #1: LACTIC ACID With potassium carbonate In water at 20 - 90℃; for 1h; Stage #2: 1-bromo-butane at 20 - 40℃; for 8h; Reagent/catalyst; Temperature; | 97.5% |
LACTIC ACID
butan-1-ol
A
2-lactoyloxy-propionic acid butyl ester
B
n-butyl lactate
Conditions | Yield |
---|---|
aluminium(III) triflate In iso-tridecanol; di-isopropyl ether; water at 66 - 120℃; under 150.015 - 7500.75 Torr; for 6h; Conversion of starting material; | A 4% B 95% |
n-butyl lactate
Conditions | Yield |
---|---|
With dibromotriphenylphosphorane In dichloromethane at -50℃; for 3h; | 94% |
Conditions | Yield |
---|---|
With tin (IV) chloride pentahydrate at 110℃; for 6h; | 88.4% |
Conditions | Yield |
---|---|
aluminium(III) triflate at 120 - 140℃; under 37.5038 - 7500.75 Torr; for 1.5 - 6h; Conversion of starting material; | 70.9% |
zirconium(IV) triflate at 120 - 140℃; under 37.5038 - 7500.75 Torr; for 1 - 6h; Conversion of starting material; | 46.6% |
Conditions | Yield |
---|---|
Sn-BEA at 160℃; under 15001.5 Torr; Inert atmosphere of argon; | A 26% B 8% |
Sn-BEA at 160℃; for 20h; Inert atmosphere; autoclave; | A 26% B 8% |
LACTIC ACID
n-butyl lactate
Conditions | Yield |
---|---|
at 100 - 120℃; unter vermindertem Druck; man kocht 25 Stdn. mit Butylalkohol; |
Conditions | Yield |
---|---|
With 2-(diethylamine)ethanethiol | |
With titanium-silicon molecular sieve TS-1; tin-silicon molecular sieve Sn-Beta at 60℃; for 7h; |
Conditions | Yield |
---|---|
With sulfuric acid; benzene unter azeotropem Abdestillieren des Reaktionswassers; | |
With sulfuric acid; toluene unter azeotropem Abdestillieren des Reaktionswassers; |
Conditions | Yield |
---|---|
With sulfuric acid; benzene unter azeotropem Abdestillieren des Reaktionswassers; | |
With sulfuric acid; toluene unter azeotropem Abdestillieren des Reaktionswassers; |
Conditions | Yield |
---|---|
In diethyl ether Heating; |
Conditions | Yield |
---|---|
With water und Entfernen des entstehenden Wassers und Ammoniaks; |
Glyceraldehyde
butan-1-ol
A
1,1-dibutoxy-2-propanone
B
n-butyl lactate
Conditions | Yield |
---|---|
tin(IV) chloride at 90℃; for 1h; | A n/a B 82 % Chromat. |
2-oxopropanal
butan-1-ol
A
1,1-dibutoxy-2-propanone
B
n-butyl lactate
Conditions | Yield |
---|---|
tin(ll) chloride at 90℃; for 3h; | A n/a B 78 % Chromat. |
dihydroxyacetone
butan-1-ol
A
1,1-dibutoxy-2-propanone
B
n-butyl lactate
Conditions | Yield |
---|---|
tin(IV) chloride at 90℃; for 1h; | A n/a B 91 % Chromat. |
With Zeolite USY CBV 600 at 109.84℃; for 4h; Autoclave; | A 28 %Chromat. B 71 %Chromat. |
Conditions | Yield |
---|---|
aluminium(III) triflate at 125 - 145℃; under 37.5038 - 7500.75 Torr; Conversion of starting material; |
Conditions | Yield |
---|---|
In diethylene glycol dimethyl ether |
n-butyl pyruvate
n-butyl lactate
Conditions | Yield |
---|---|
With Streptomyces avermitilis α-keto ester reductase I, Mr 71.6 kDa by gel filtration; NAD at 37℃; for 6h; aq. phosphate buffer; |
Conditions | Yield |
---|---|
for 24h; |
A
furfural
B
5-Methylfurfural
C
3-methyl-furan-2,4-dione
D
2-(diethoxymethyl)furan
E
n-butyl lactate
F
acetic acid butyl ester
G
levulinic acid methyl ester
H
methyl 3-hydroxyhexanoate
I
methyl 3-methylenecyclopentane-1-carboxylate
J
levulinic acid
Conditions | Yield |
---|---|
With 1-methyl-3-(4-sulfobutyl)-1H-imidazol-3-ium hydrogensulfate; 1-butyl-3-methylimidazolium chloride In methanol; hexane at 19.84 - 199.84℃; pH=0.09; Mechanism; Reagent/catalyst; Temperature; pH-value; Autoclave; Inert atmosphere; chemoselective reaction; | A n/a B n/a C n/a D 45.8 %Chromat. E n/a F n/a G n/a H n/a I n/a J n/a |
Conditions | Yield |
---|---|
Stage #1: D-xylose With sodium hydroxide In water for 4h; Heating; Stage #2: butan-1-ol With hydrogenchloride In water at 106℃; for 4h; pH=1; Dean-Stark; Reflux; | 35.6 %Chromat. |
1,6-anhydro-2,2',3,3',4',6'-hexa-O-acetyl-β-D-lactose
n-butyl lactate
Conditions | Yield |
---|---|
In [(2)H6]acetone |
n-butyl lactate
Conditions | Yield |
---|---|
Stage #1: lactic acid-triethylamine complex at 170℃; Dean-Stark; Stage #2: butan-1-ol for 24h; Reflux; | 42 %Chromat. |
Conditions | Yield |
---|---|
With tungsten(VI) oxide at 160℃; under 3750.38 Torr; for 5h; Reagent/catalyst; Inert atmosphere; Autoclave; | 23 %Chromat. |
Conditions | Yield |
---|---|
at 180℃; for 8h; Time; |
n-butyl lactate
n-butyl pyruvate
Conditions | Yield |
---|---|
With hydrogenchloride; sodium hypobromide In dichloromethane; water at 25℃; for 5h; | 96% |
With silica gel supported bis(trimethylsilyl) chromate In dichloromethane at 25℃; for 0.333333h; | 83% |
With air at 180℃; | |
Oxidation; |
Conditions | Yield |
---|---|
With hydrogenchloride; sodium thiosulfate In dichloromethane | 94% |
With sodium hydrogencarbonate; sodium thiosulfate In dichloromethane; water | 132.5g (92%yield) |
Conditions | Yield |
---|---|
With oxalic acid diethyl ester at 130℃; under 760.051 Torr; for 5h; Reagent/catalyst; Temperature; | 90.2% |
Conditions | Yield |
---|---|
iodine for 15h; Heating; | 90% |
Conditions | Yield |
---|---|
With Amberlyst 15 hydrogen form for 2h; Reagent/catalyst; Reflux; | 88% |
Conditions | Yield |
---|---|
With hydrogen In ethanol at 220℃; under 37503.8 Torr; for 12h; Catalytic behavior; | 67% |
With hydrogen at 220℃; under 37503.8 Torr; for 12h; | 67% |
n-butyl lactate
carbon monoxide
Conditions | Yield |
---|---|
With di(rhodium)tetracarbonyl dichloride; tris(pentafluorophenyl)phosphine In 1,2-dichloro-benzene at 130℃; under 760.051 Torr; for 36h; Glovebox; | 67% |
Conditions | Yield |
---|---|
With tin(II) chloride dihdyrate at 200℃; under 20627.1 Torr; for 3h; | 60% |
Conditions | Yield |
---|---|
With immobilized lipase B from Candida antarctica In neat (no solvent) at 65℃; for 9h; Temperature; Resolution of racemate; Large scale; Enzymatic reaction; enantioselective reaction; | A 48% B 48% |
1. | skn-rbt 500 mg/24H MOD | FCTXAV Food and Cosmetics Toxicology. 17 (1979),727. | ||
2. | scu-rat LD50:12 g/kg | NPIRI* Raw Material Data Handbook, Vol.1: Organic Solvents, 1974. 1 (1974),15. | ||
3. | ipr-mus LDLo:200 mg/kg | CBCCT* “Summary Tables of Biological Tests“ National Research Council Chemical-Biological Coordination Center. 7 (1955),690. | ||
4. | scu-mus LD50:11,000 mg/kg | FCTXAV Food and Cosmetics Toxicology. 17 (1979),727. |
Poison by intraperitoneal route. A skin irritant. Toxic concentration in air for humans is about 4 ppm. Flammable when exposed to heat or flame; can react with oxidizing materials. To fight fire, use alcohol foam, foam, CO2, dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes. See also ESTERS, n-BUTYL ALCOHOL, and LACTIC ACIDLACTIC ACID.
Safety Information for n-Butyl lactate(138-22-7)
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-37/39
WGK Germany 2
RTECS OD4025000
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