ChemicalBook--->CAS DataBase List--->955406-36-7

955406-36-7

955406-36-7 Structure

955406-36-7 Structure
IdentificationBack Directory
[Name]

3-BENZYLOXYCARBONYLAMINO-CYCLOHEXANOL
[CAS]

955406-36-7
[Synonyms]

Benzyl (3-hydroxycyclohexyl)
3-BENZYLOXYCARBONYLAMINO-CYCLOHEXANOL
Benzyl (3-hydroxycyclohexyl)carbamate
(3-hydroxy-cyclohexyl)-carbamic acid benzyl ester
Carbamic acid,N-(3-hydroxycyclohexyl)-, phenylmethyl ester
[Molecular Formula]

C14H19NO3
[MDL Number]

MFCD08061945
[MOL File]

955406-36-7.mol
[Molecular Weight]

249.31
Chemical PropertiesBack Directory
[Boiling point ]

427.6±44.0 °C(Predicted)
[density ]

1.17±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

12.11±0.40(Predicted)
[Appearance]

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

3-BENZYLOXYCARBONYLAMINO-CYCLOHEXANOL(955406-36-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-Aminocyclohexanol

6850-39-1

Benzyl chloroformate

501-53-1

3-BENZYLOXYCARBONYLAMINO-CYCLOHEXANOL

955406-36-7

General procedure for the synthesis of benzyl (3-hydroxycyclohexyl) carbamate from 3-aminocyclohexanol and benzyl chloroformate: 3-hydroxycyclohexylamine (10 g, 86.96 mmol), potassium carbonate (18 g, 130 mmol), ethyl acetate (150 mL), and water (70 mL) were mixed, followed by the addition of benzyl chloroformate (22.17 g, 130 mmol). The reaction mixture was stirred at room temperature for 12 hours. Upon completion of the reaction, the organic layer was separated, dried over anhydrous sodium sulfate, filtered and concentrated. To the concentrated residue diethyl ether was added, a white precipitate was precipitated, filtered and air-dried to give benzyl (3-hydroxycyclohexyl) carbamate 19.1 g in 88% yield. Mass spectrum (m/z): 250 (M+).

[References]

[1] Patent: US2009/111800, 2009, A1. Location in patent: Page/Page column 40
[2] Patent: WO2014/145512, 2014, A2. Location in patent: Page/Page column 136; 137
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