4-CHLORO-2-BUTANONE
4-CHLORO-2-BUTANONE Basic information
- Product Name:
- 4-CHLORO-2-BUTANONE
- Synonyms:
-
- B-CHLOROETHYL METHYL KETONE
- TIMTEC-BB SBB007824
- 4-chlorobutan-2-one
- 4-Chloro-2-butanone, Pract.
- Einecs 228-680-6
- 2-Butanone, 4-chloro-
- 2-Chloroethylmethylketone
- 4-CHLORO-2-BUTANONE
- CAS:
- 6322-49-2
- MF:
- C4H7ClO
- MW:
- 106.55
- EINECS:
- 228-680-6
- Product Categories:
-
- Fine Chemical
- API Intermediate
- Mol File:
- 6322-49-2.mol
4-CHLORO-2-BUTANONE Chemical Properties
- Boiling point:
- 146℃
- Density
- 1.033
- refractive index
- 1.4299-1.4334
- Flash point:
- 45℃
- storage temp.
- Inert atmosphere,Store in freezer, under -20°C
- solubility
- Chloroform, Ethyl Acetate (Slightly)
- form
- Oil
- color
- Black
- InChI
- InChI=1S/C4H7ClO/c1-4(6)2-3-5/h2-3H2,1H3
- InChIKey
- MAGOYBJJLVSJIC-UHFFFAOYSA-N
- SMILES
- CC(=O)CCCl
- LogP
- 0.666 (est)
4-CHLORO-2-BUTANONE Usage And Synthesis
Chemical Properties
Liquid. Boiling point 123°C (98 kPa, decomposition), 55°C (2.13 kPa), relative density 1.068 (23/4°C), refractive index 1.4284 (23°C).
Uses
4-Chloro-2-butanone acts as a reagent for the preparation of pyrrolopyrazine derivatives as selective spleen tyrosine kinase inhibitors.
Application
4-Chloro-2-butanone is a reagent for Robinson annulation; often interchangeable with methyl vinyl ketone and the corresponding Mannich base 4-dialkylamino-2-butanone.
Synthesis Reference(s)
Synthetic Communications, 26, p. 3479, 1996 DOI: 10.1080/00397919608003752
Synthesis
590-90-9
6322-49-2
General procedure for the synthesis of β-chlorobutanone from 4-hydroxy-2-butanone: 4-hydroxy-2-butanone (0.881 g, 10 mmol), dichloromethane (2 ml), and thionyl chloride (1.46 ml, 20 mmol) were added in a reaction flask and the reaction was stirred at room temperature overnight. Upon completion of the reaction, the solvent was removed by rotary evaporator and the residue was dried with a stream of nitrogen to give 2-chlorobutan-2-one (1.06 g). The product was characterized by 1H-NMR (400 MHz, DMSO-d6): δ 2.12 (s, 3H), 2.94 (t, 2H), 3.74 (t, 2H).
References
[1] Angewandte Chemie - International Edition, 2012, vol. 51, # 27, p. 6713 - 6716
[2] Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1936, vol. 202, p. 1687
[3] Zhurnal Obshchei Khimii, 1938, vol. 8, p. 909
[4] Chem. Zentralbl., 1939, vol. 110, # I, p. 4953
[5] Patent: WO2015/169999, 2015, A1. Location in patent: Page/Page column 63
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