ChemicalBook--->CAS DataBase List--->123469-92-1

123469-92-1

123469-92-1 Structure

123469-92-1 Structure
IdentificationBack Directory
[Name]

ethyl-2,2-dimethyl-7-bromoheptanoate
[CAS]

123469-92-1
[Synonyms]

ETC-1002 intermediate 2
Bempedoic Acid Impurity 9
Bempedoic acid intermediate
ethyl 7-bromo-2,2-dimethylheptanoate
ethyl-2,2-dimethyl-7-bromoheptanoate
7-Bromo-2,2-dimethylheptanoic acid ethyl ester
Heptanoic acid, 7-bromo-2,2-dimethyl-, ethyl ester
[Molecular Formula]

C11H21BrO2
[MDL Number]

MFCD27942427
[MOL File]

123469-92-1.mol
[Molecular Weight]

265.19
Chemical PropertiesBack Directory
[Boiling point ]

106-108 °C(Press: 0.01 Torr)
[density ]

1.169±0.06 g/cm3(Predicted)
[vapor pressure ]

0.0±0.6 mmHg at 25°C
[refractive index ]

1.463
[Fp ]

146.4±13.0 °C
[storage temp. ]

Store at room temperature
[Appearance]

Colorless to light yellow Liquid
[InChI]

InChI=1S/C11H21BrO2/c1-4-14-10(13)11(2,3)8-6-5-7-9-12/h4-9H2,1-3H3
[InChIKey]

SYRIIFZUZOIRNU-UHFFFAOYSA-N
[SMILES]

C(OCC)(=O)C(C)(C)CCCCCBr
[LogP]

3.92
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[RIDADR ]

UN2810
[HazardClass ]

6.1
[HS Code ]

2915907098
Hazard InformationBack Directory
[Description]

Ethyl 7-bromo-2,2-dimethylheptanoate is an important raw material in the synthesis route of bepetidic acid. Bempedoic acid, whose chemical name is 8-hydroxy-2,2,14,14-tetramethylpentadecanedioic acid, also known as ETC-1002, is a new type of lipid developed by the American EsperionTherapeutic company Quality regulation small molecule drugs. As one of the company's main drug candidates, its targets are liver adenosine triphosphate-citrate lyase (ACL) and adenosine monophosphate-activated protein kinase (AMPK).
[Uses]

Ethyl-2,2-dimethyl-7-bromoheptanoate can be used as an intermediate in organic synthesis, mainly used in laboratory research and development and chemical production processes.
[Synthesis]

Synthesis_123469-92-1
The specific embodiment of the present invention is as follows: prepare 19.4g (167mmol) of ethyl isobutyrate in 216mL solution of tetrahydrofuran with a mass concentration of 10%, connect to metering pump 1; prepare 84mL (168mmol) of 2.0M n-butyllithium solution, connect to meter Pump 2; configure 1,5-dibromopentane 80.0g (348mmol) tetrahydrofuran 100mL solution, mass concentration is 63%, connected to metering pump 3.Configure 300mL of 1N hydrochloric acid solution and connect to metering pump 4.Set continuous flow precooler 1, the circulating temperature is 0, and reach stability; set continuous flow precooler 2, the circulating temperature is 0, and reach stability; set continuous flow precooler 3, and the circulating temperature is 0, and reach stability; set continuous flow precooler 4, cycle temperature is 0, and reach stability;Set the flow rate of metering pump 1 to 65.0ml/min, set the flow rate of metering pump 2 to 25.0ml/min, set the flow rate of metering pump 3 to 30.0ml/min, and set the flow rate of metering pump 4 to 90.0ml/min.Turn on the metering pump 1 and metering pump 2 at the same time. After 60s of operation, turn on the metering pump 3, and after 60s of operation, turn on the metering pump 4 to collect the outflowing reaction liquid in the storage tank.After the operation is completed, separate the liquids, collect the upper organic phase, concentrate under reduced pressure at P=-0.08MPa, T=45??C to remove low-boiling solvents, and then rectify under reduced pressure at P=5mmHg and T=70??C to obtain 38.4 g.The obtained product is a colorless liquid with a GC purity of 98.6% and a yield of 87%.
Spectrum DetailBack Directory
[Spectrum Detail]

ethyl-2,2-dimethyl-7-bromoheptanoate(123469-92-1)1HNMR
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