Methyl 3-oxohexanoate
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
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)
Safety Information
- Safety Statements
- 24/25
- WGK Germany
- 3
- HS Code
- 2918300090
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
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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