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ChemicalBook--->CAS DataBase List--->88987-42-2

88987-42-2

88987-42-2 Structure

88987-42-2 Structure
IdentificationBack Directory
[Name]

5-BROMOPENTANOIC ACID, T-BUTYL ESTER
[CAS]

88987-42-2
[Synonyms]

tert-Butyl 5-bromovalerate
tert-butyl 5-bromopentanoate
5-BROMOPENTANOIC ACID, T-BUTYL ESTER
Pentanoic acid, 5-bromo-, 1,1-dimethylethyl ester
[Molecular Formula]

C9H17BrO2
[MDL Number]

MFCD26398445
[MOL File]

88987-42-2.mol
[Molecular Weight]

237.13
Chemical PropertiesBack Directory
[Boiling point ]

93 °C(Press: 1.6 Torr)
[density ]

1.223±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

Colorless to light yellow Liquid
[InChI]

InChI=1S/C9H17BrO2/c1-9(2,3)12-8(11)6-4-5-7-10/h4-7H2,1-3H3
[InChIKey]

UYDIIUHJHUZDME-UHFFFAOYSA-N
[SMILES]

C(OC(C)(C)C)(=O)CCCCBr
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

tert-Butyl 5-Bromovalerate is a reactant used in synthetic preparation of haptens for production of monoclonal antibodies for pyraclostrobin ELISA.
[Synthesis]

5-Bromovaleric acid

2067-33-6

tert-Butanol

75-65-0

5-BROMOPENTANOIC ACID, T-BUTYL ESTER

88987-42-2

5-Bromovaleric acid (5 g, 27.62 mmol) was dissolved in anhydrous dichloromethane (DCM), and the solution was brought to room temperature and stirred under cooling in an ice bath. N,N'-dimethylaminopyridine (DMAP, 1.68 g, 13.75 mmol) and dicyclohexylcarbodiimide (DCC, 6.83 g, 33.15 mmol) were added sequentially. After half an hour of reaction, tert-butanol (15.8 ml, 165.75 mmol) was added to the mixture. The reaction solution was stirred at room temperature overnight. After completion of the reaction, the reaction mixture was diluted with dichloromethane and washed sequentially with water and brine. The organic layer was separated, dried over anhydrous sodium sulfate and evaporated under reduced pressure to remove the solvent. The crude product was purified by silica gel column chromatography with hexane-ethyl acetate (1%) as eluent to give pure tert-butyl 5-bromopentanoate 4.1 g (62.6% yield) as a light yellow liquid.

[References]

[1] Patent: WO2015/6740, 2015, A2. Location in patent: Page/Page column 182; 183
[2] Patent: WO2016/154241, 2016, A1. Location in patent: Paragraph 670; 671
[3] European Journal of Organic Chemistry, 2018, vol. 2018, # 37, p. 5180 - 5192
[4] Patent: KR101569966, 2015, B1. Location in patent: Paragraph 0145; 0146
[5] Patent: WO2011/53519, 2011, A1. Location in patent: Page/Page column 27-28
Spectrum DetailBack Directory
[Spectrum Detail]

5-BROMOPENTANOIC ACID, T-BUTYL ESTER(88987-42-2)1HNMR
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