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Methyl 3-oxohexanoate

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Methyl 3-oxohexanoate Basic information

Product Name:
Methyl 3-oxohexanoate
Synonyms:
  • 3-OXOHEXANOIC ACID METHYL ESTER
  • 3-KETOHEXANOIC ACID METHYL ESTER
  • 3-KETO-N-HEXANOIC ACID METHYL ESTER
  • METHYL 3-OXOHEXANOATE
  • METHYL 3-OXOCAPROATE
  • METHYL BUTYRYLACETATE
  • BEM
  • BUTYRYLACETIC ACID METHYL ESTER
CAS:
30414-54-1
MF:
C7H12O3
MW:
144.17
EINECS:
250-185-9
Product Categories:
  • BUILDING BLOCKS
Mol File:
30414-54-1.mol
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Methyl 3-oxohexanoate Chemical Properties

Melting point:
-43°C
Boiling point:
85-88 °C25 hPa(lit.)
Density 
1.017 g/mL at 20 °C(lit.)
vapor pressure 
40Pa at 20℃
refractive index 
1.4260
Flash point:
90°C
storage temp. 
2-8°C
pka
10.67±0.46(Predicted)
form 
clear liquid
color 
Colorless to Almost colorless
Water Solubility 
33g/L at 20℃
BRN 
636165
LogP
0.877 at 20℃
CAS DataBase Reference
30414-54-1(CAS DataBase Reference)
NIST Chemistry Reference
Hexanoic acid, 3-oxo-, methyl ester(30414-54-1)
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Safety Information

Safety Statements 
24/25
WGK Germany 
3
HS Code 
2918300090

MSDS

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Methyl 3-oxohexanoate Usage And Synthesis

Uses

Methyl 3-oxohexanoate (Methyl Butyrylacetate) is an organic compound commonly used in the manufacture of fragrances, drugs, and other chemicals. It can be used as a condensation reagent, a diazotization reagent and an addition reagent, and it plays a catalytic role in some organic synthesis reactions, and can also play a role in some drug synthesis. In addition, the compound is widely used in the food industry, for example in products such as juices, beer and confectionery.

Synthesis

Butyl chloride (18.0 g, 168.94 mmol) in CHCl3 (50 mL) was added dropwise to a stirred solution of 2,2-dimethyl-1,3-dioxane-4,6-dione (22.14 g, 153.58 mmol) and pyridine (25.0 mL, 307.2 mmol) in CHCl3 (250 mL) at 0 ??C and stirred for 1 hour. The reaction mixture was allowed to warm to ambient temperature and stirred overnight. Aqueous 1N HCl (150 mL) was added and the resulting mixture was extracted with CHCl3 (3 x 150 mL). The combined organic layers were washed with water (2 x 100 mL), dried over Na2SO4, filtered and concentrated. CH3OH (250 mL) was added and the solution was heated to 80 ??C and refluxed for 3 hours. Concentrated under reduced pressure and distilled to give the title compound as a yellow liquid in yield (17.6 g).

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