ChemicalBook--->CAS DataBase List--->210962-44-0

210962-44-0

210962-44-0 Structure

210962-44-0 Structure
IdentificationBack Directory
[Name]

tert-Butyl 4-(4-(ethoxycarbonyl)phenoxy)piperidine-1-carboxylate
[CAS]

210962-44-0
[Synonyms]

Ethyl 4-[(1-Boc-4-piperidyl)oxy]benzoate
tert-Butyl 4-(4-(ethoxycarbonyl)phenoxy)piperidine-1-carboxylate
1-Piperidinecarboxylic acid, 4-[4-(ethoxycarbonyl)phenoxy]-, 1,1-dimethylethyl ester
[Molecular Formula]

C19H27NO5
[MDL Number]

MFCD13184258
[MOL File]

210962-44-0.mol
[Molecular Weight]

349.42
Chemical PropertiesBack Directory
[Boiling point ]

459.0±35.0 °C(Predicted)
[density ]

1.132±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

-2.51±0.40(Predicted)
[Appearance]

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

tert-Butyl 4-(4-(ethoxycarbonyl)phenoxy)piperidine-1-carboxylate(210962-44-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

Ethylparaben

120-47-8

N-BOC-4-Hydroxypiperidine

109384-19-2

tert-Butyl 4-(4-(ethoxycarbonyl)phenoxy)piperidine-1-carboxylate

210962-44-0

Step 1: At 0°C, DEAD (12.3 mL, 27.08 mmol, 40% toluene solution) was slowly added dropwise to THF containing ethyl 4-hydroxybenzoate (3.0 g, 18.05 mmol), N-Boc-4-hydroxypiperidine (4.72 g, 23.47 mmol), and triphenylphosphine (6.16 g, 23.47 mmol) ( 40 mL) solution. The reaction mixture was stirred at 0 °C to room temperature for 24 hours. Subsequently, the reaction solution was concentrated under reduced pressure. The residue was diluted with EtOAc, washed sequentially with 1N NaOH and saturated saline, and the organic phase was dried over anhydrous Na2SO4 and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (elution gradient: 0→30% EtOAc/hexane) to afford tert-butyl 4-(4-(ethoxycarbonyl)phenoxy)piperidine-1-carboxylate (5.4 g, 15.45 mmol, 85.6% yield) as a colorless oil.ESIMS m/z: 372.1 [M+Na]+ (calculated value C19H27NO5Na. 372.1).

[References]

[1] Patent: US2017/313682, 2017, A1. Location in patent: Paragraph 0702; 0703
[2] Patent: EP1757594, 2007, A1. Location in patent: Page/Page column 72-73
[3] Journal of Medicinal Chemistry, 2003, vol. 46, # 10, p. 1845 - 1857
[4] Patent: WO2007/106705, 2007, A1. Location in patent: Page/Page column 115
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