ChemicalBook--->CAS DataBase List--->55736-04-4

55736-04-4

55736-04-4 Structure

55736-04-4 Structure
IdentificationBack Directory
[Name]

1-(2-Chloro-6-hydroxyphenyl)ethanone
[CAS]

55736-04-4
[Synonyms]

oro-6-hydroxyphenyL
1-(2-Chloro-6-hydroxyphenyl)
2'-Chloro-6'-hydroxyacetophenone
1-(2-Chloro-6-hydroxyphenyl)ethanone
Ethanone, 1-(2-chloro-6-hydroxyphenyl)-
1-(2-Chloro-6-hydroxyphenyl)ethan-1-one 97+%
[Molecular Formula]

C8H7ClO2
[MDL Number]

MFCD00218550
[MOL File]

55736-04-4.mol
[Molecular Weight]

170.59
Chemical PropertiesBack Directory
[Boiling point ]

225.4±20.0 °C(Predicted)
[density ]

1.298±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

9.20±0.10(Predicted)
[Appearance]

Off-white to yellow Solid
[InChI]

InChI=1S/C8H7ClO2/c1-5(10)8-6(9)3-2-4-7(8)11/h2-4,11H,1H3
[InChIKey]

RUSSVKYJPIADHS-UHFFFAOYSA-N
[SMILES]

C(=O)(C1=C(O)C=CC=C1Cl)C
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2914500090
Hazard InformationBack Directory
[Uses]

1-(2-Chloro-6-hydroxyphenyl)ethanone is used for synthesis and structure-activity relationship of novel spiropiperidine-based stearoyl-CoA desaturase-1 inhibitors.
[Preparation]

Preparation by diazotization of 2-amino-6-chloro-acetophenone, followed by hydrolysis of the obtained diazonium salt (55%).
[Synthesis]

2-CHLORO-6-HYDROXYBENZONITRILE

89999-90-6

Methylmagnesium Bromide

75-16-1

1-(2-Chloro-6-hydroxyphenyl)ethanone

55736-04-4

1. To a solution of 2-chloro-6-hydroxybenzonitrile (614 mg, 4 mmol) in tetrahydrofuran (THF, 10 mL) under argon protection is slowly added a solution of methylmagnesium bromide in toluene/THF (3:1, 1.4 M, 6.4 mL, 9 mmol). Note: Gas escapes during the reaction. 2. Stir the reaction mixture at room temperature until the escape of gas ceases. 3. Transfer the reaction mixture to a sealed tube and stir overnight at 65°C. 4. 4. upon completion of the reaction, the reaction is quenched with water and acidified with aqueous hydrochloric acid. 5. The organic layer containing 1-(2-chloro-6-hydroxyphenyl)ethanone was extracted with dichloromethane (DCM). 6. The product was purified by column chromatography using dichloromethane/hexane (1:1) as eluent to afford 1-(2-chloro-6-hydroxyphenyl)ethanone (100 mg, 15% yield).

[References]

[1] Patent: WO2010/56631, 2010, A1. Location in patent: Page/Page column 132-134
Spectrum DetailBack Directory
[Spectrum Detail]

1-(2-Chloro-6-hydroxyphenyl)ethanone(55736-04-4)1HNMR
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