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ethyl 1-acetylcyclopropanecarboxylate

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ethyl 1-acetylcyclopropanecarboxylate manufacturers

ethyl 1-acetylcyclopropanecarboxylate Basic information
Product Name:ethyl 1-acetylcyclopropanecarboxylate
Synonyms:ethyl 1-acetylcyclopropanecarboxylate;1-Acetyl-cyclopropanecarboxylic acid ethyl ester;Ethyl 1-acetylcyclopropane-1-carboxylate;thyl 1-acetylcyclopropanecarboxylate;1-acetyl-1-cyclopropanecarboxylic acid ethyl ester;Cyclopropanecarboxylic acid, 1-acetyl-, ethyl ester;Cyclopropanecarboxylic acid, 1-acetyl-, ethyl ester (8CI, 9CI, ACI);1-acetyl-Cyclopropanecarboxylic acid ethyl ester (8CI 9CI ACI)
CAS:32933-03-2
MF:C8H12O3
MW:156.18
EINECS:628-471-3
Product Categories:
Mol File:32933-03-2.mol
ethyl 1-acetylcyclopropanecarboxylate Structure
ethyl 1-acetylcyclopropanecarboxylate Chemical Properties
Boiling point 42-44 °C(Press: 2 Torr)
density 1.139±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form solid
AppearanceColorless to light yellow Liquid
InChIInChI=1S/C8H12O3/c1-3-11-7(10)8(4-5-8)6(2)9/h3-5H2,1-2H3
InChIKeyDISZFIFAESWGBI-UHFFFAOYSA-N
SMILESC1(C(C)=O)(C(OCC)=O)CC1
Safety Information
WGK Germany WGK 3
HS Code 2902190000
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
MSDS Information
ethyl 1-acetylcyclopropanecarboxylate Usage And Synthesis
Usesethyl 1-methyl cyclopropanecarboxylate is an important pharmaceutical intermediate used in the addition of cyclopropane.
Synthesis
Ethyl acetoacetate

141-97-9

1,2-Dibromoethane

106-93-4

ethyl 1-acetylcyclopropanecarboxylate

32933-03-2

Step 1) Synthesis of ethyl 1-acetylcyclopropanecarboxylate: To a solution of ethyl 3-oxobutanoate (26 g, 200 mmol) in acetone (500 mL) was added potassium carbonate (82.8 g, 600 mmol) followed by 1,2-dibromoethane (45.12 g, 240 mmol). The reaction mixture was refluxed for 24 hours. After completion of the reaction, the mixture was filtered and the filtrate was concentrated under vacuum. The residue was purified by silica gel column chromatography with an eluent ratio of 1:50 (v/v) ethyl acetate/hexane to afford the target compound ethyl 1-acetylcyclopropanecarboxylate as a colorless oil (18.7 g, 60% yield). Mass spectrum (ESI, cation mode) m/z: 157 (M+1); 1H NMR (400 MHz, CDCl3) δ: 1.25-1.29 (t, J=7.2 Hz, 3H), 1.45 (s, 4H), 2.45 (s, 3H), 4.18-4.20 (q, 2H).

References[1] Tetrahedron Letters, 2005, vol. 46, # 4, p. 635 - 638
[2] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2004, vol. 43, # 2, p. 420 - 422
[3] Tetrahedron Asymmetry, 2010, vol. 21, # 5, p. 631 - 635
[4] Journal of Organic Chemistry, 2011, vol. 76, # 8, p. 2807 - 2813
[5] Chemistry of Heterocyclic Compounds (New York, NY, United States), 1983, vol. 19, # 6, p. 644 - 650
ethyl 1-acetylcyclopropanecarboxylate Preparation Products And Raw materials
Raw materialsEthyl acetoacetate-->1,2-Dibromoethane-->Acetone-->Potassium carbonate
Tag:ethyl 1-acetylcyclopropanecarboxylate(32933-03-2) Related Product Information
Methyl 1-acetylcyclopropylcarboxylate Ethyl 1-isobutyrylcyclopropanecarboxylate Diethyl 1,1-cyclopropanedicarboxylate Cyclopropanecarboxylic acid, 1-acetyl- Ethanone, 1-[1-(hydroxymethyl)cyclopropyl]- (9CI) Cyclopropanecarboxylic acid, 1-acetyl-, 1,1-dimethylethyl ester