63095-51-2

  • Product Name:Brivaracetam Impurity
  • Molecular Formula:C7H12O2
  • Purity:99%
  • Molecular Weight:128.171
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Product Details;

CasNo: 63095-51-2

Molecular Formula: C7H12O2

Manufacturer supply high quality Brivaracetam Impurity 63095-51-2 with GMP standards

  • Molecular Formula:C7H12O2
  • Molecular Weight:128.171
  • Boiling Point:226.3±8.0 °C(Predicted) 
  • PSA:26.30000 
  • Density:0.983±0.06 g/cm3(Predicted) 
  • LogP:1.34960 

63095-51-2 Relevant articles

Preparation method of brivaracetam intermediate

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Paragraph 0025; 0070-0071, (2021/09/04)

The invention provides a preparation met...

Preparation method of brivaracetam intermediate

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Paragraph 0102-0107, (2021/06/12)

The invention relates to a preparation m...

COMPOUND AND USE THEREOF IN SYNTHESIS OF BRIVARACETAM INTERMEDIATE AND CRUDE DRUG

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Page/Page column 0095, (2021/08/27)

The present application provides a compo...

Synthesis and olfactory evaluation of optically active β-alkyl substituted γ-lactones and whiskey lactone analogues

Kato, Daiki,Kawasaki, Masashi,Morita, Yuko,Okada, Takuya,Tanaka, Yasuo,Toyooka, Naoki

, (2020/02/22)

Optically active β-alkyl substituted γ-l...

63095-51-2 Process route

4-propyl-5H-furan-2-one
21963-27-9

4-propyl-5H-furan-2-one

(+)-(R)-4-propyl-4,5-dihydrofuran-2(3H)-one
63095-51-2

(+)-(R)-4-propyl-4,5-dihydrofuran-2(3H)-one

Conditions
Conditions Yield
With bis(η5-cyclopentadienyl)ruthenium; (R,R)-(+)-2,2'-isopropylidene bis(4-isopropyl-2-oxazoline); hydrogen; In methanol; at 50 ℃; under 15001.5 Torr; Temperature; Pressure; Solvent; Reagent/catalyst; Autoclave;
93%
With water; (S)-(1,1'-binaphthalene)-2,2'-diylbis(diphenylphosphine); copper(l) chloride; sodium t-butanolate; In toluene; tert-butyl alcohol; at 0 - 30 ℃; Inert atmosphere;
79.63%
Multi-step reaction with 2 steps
1: palladium 10% on activated carbon; hydrogen / methanol / 4 h / 20 °C / 9000.9 Torr
2: sodium hydroxide / water / 2 h / 30 °C
With palladium 10% on activated carbon; hydrogen; sodium hydroxide; In methanol; water;
Multi-step reaction with 4 steps
1: palladium 10% on activated carbon; hydrogen / ethanol / 9 h / 20 °C / 225.02 - 375.04 Torr / Large scale
2: sodium hydroxide / ethanol / 1 h / 20 °C / Large scale
3: 0.5 h / 20 °C / Large scale
4: hydrogenchloride / water / 3 h / 20 - 60 °C / Large scale
With hydrogenchloride; palladium 10% on activated carbon; hydrogen; sodium hydroxide; In ethanol; water;
C<sub>7</sub>H<sub>14</sub>O<sub>3</sub>

C7H14O3

(+)-(R)-4-propyl-4,5-dihydrofuran-2(3H)-one
63095-51-2

(+)-(R)-4-propyl-4,5-dihydrofuran-2(3H)-one

Conditions
Conditions Yield
With hydrogenchloride; In water; at 20 ℃; pH=3;
77%
With toluene-4-sulfonic acid; In toluene; for 20h; Reflux;
12 g
With toluene-4-sulfonic acid; In toluene; Reflux;
7.8 g
With toluene-4-sulfonic acid; In toluene; Reflux;
12 g
With toluene-4-sulfonic acid; In toluene; at 20 ℃; Reflux;
12 g
With trifluoroacetic acid; In toluene; at 20 - 30 ℃;

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