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3-Chloropropiophenone

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3-Chloropropiophenone Basic information
Product Name:3-Chloropropiophenone
Synonyms:3-CHLORO-1-PHENYL-1-PROPANONE;3-CHLORO-1-OXO-1-PHENYLPROPANE;B-CHLOROPROPIOPHENONE;BETA-CHLOROPROPIOPHENONE;3-Chloropropiophenone98%;Chloropropiophenone, 98+%;beta-Chloropropiophenone,98+%;3-Chloropropiophenone, tech., 90%
CAS:936-59-4
MF:C9H9ClO
MW:168.62
EINECS:213-317-6
Product Categories:Building Blocks;C9;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks;Ketones;Aromatics, Impurities, Intermediates;API
Mol File:936-59-4.mol
3-Chloropropiophenone Structure
3-Chloropropiophenone Chemical Properties
Melting point 48-50 °C(lit.)
Boiling point 113-115 °C4 mm Hg(lit.)
density 1.1115 (rough estimate)
refractive index 1.5350 (estimate)
Fp >230 °F
storage temp. Inert atmosphere,Room Temperature
solubility Chloroform (Slightly), Methanol (Slightly)
form Solid
color Off-White to Pale Yellow
Water Solubility Insoluble
BRN 2043580
Stability:Stable. Incompatible with strong bases, strong oxidizing agents.
InChI1S/C9H9ClO/c10-7-6-9(11)8-4-2-1-3-5-8/h1-5H,6-7H2
InChIKeyKTJRGPZVSKWRTJ-UHFFFAOYSA-N
SMILESClCCC(=O)c1ccccc1
CAS DataBase Reference936-59-4(CAS DataBase Reference)
NIST Chemistry Reference1-Propanone, 3-chloro-1-phenyl-(936-59-4)
EPA Substance Registry System1-Propanone, 3-chloro-1-phenyl- (936-59-4)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 37/39-26-24/25
WGK Germany 3
TSCA TSCA listed
HS Code 29147000
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
3-Chloro-1-phenyl-1-propanone English
SigmaAldrich English
ACROS English
ALFA English
3-Chloropropiophenone Usage And Synthesis
Description3-Chloropropiophenone is a chiral compound that is used as an antidepressant drug. It was first synthesized in the 1950s and has been studied extensively for its pharmacological effects. It is a racemic mixture of two enantiomers, one of which is active and the other inactive. The active enantiomer binds to serotonin receptors and inhibits the reuptake of serotonin, which leads to an increase in serotonin levels. The inactive enantiomer does not bind to serotonin receptors and does not inhibit the reuptake of serotonin. 3-Chloropropiophenone has been shown to be effective when administered at an optimum concentration of 5 milligrams per kilogram body weight.
Chemical Propertiesfaintly yellow to tan crystalline powder
Uses3-Chloropropiophenone is an Impurity of Fluoxetine (F597100).
Uses3-Chloropropiophenone was used in the asymmetric reduction of (S)-3-chloro-1-phenylpropanol using preheated Candida utilis cells immobilized in calcium alginate gel beads. It was also used in the synthesis of (R)-3-chloro-1-phenyl-1-propanol via asymmetric reduction using in-situ generated oxazaborolidine catalyst derived from (S)-α,α-diphenylprolinol. It is a precursor of phenyl vinyl ketone.
Synthesis Adding 3' -chlorobenzene acetone and levorotatory prolinol into 95% ethanol and stirring; cooling after the reaction liquid is wholly dissolved; adding potassium borohydride into the reaction solution in batches, and preserving heat after adding; heating the reaction solution for reflux reaction, and concentrating the reaction solution under reduced pressure; adding n-hexane into the reaction solution, heating, and adding active carbon for heat preservation and decoloration; filtering the reaction solution, leaching a filter cake by using normal hexane, and collecting filtrate; crystallizing and filtering the filtrate, leaching the filter cake once with n-hexane, and drying in vacuum to obtain 3-Chloropropiophenone.
References[1] Synlett, 2016, vol. 27, # 5, p. 789 - 793
[2] Journal of Organic Chemistry USSR (English Translation), 1969, vol. 5, p. 323 - 326
[3] Zhurnal Organicheskoi Khimii, 1969, vol. 5, # 2, p. 337 - 340
Tag:3-Chloropropiophenone(936-59-4) Related Product Information
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