ChemicalBook--->CAS DataBase List--->765914-78-1

765914-78-1

765914-78-1 Structure

765914-78-1 Structure
IdentificationBack Directory
[Name]

4-Boc-2-(broMoMethyl)Morpholine
[CAS]

765914-78-1
[Synonyms]

4-Boc-broMoMethylMorpholine
4-Boc-2-(broMoMethyl)Morpholine
n-boc-(2)-(broMoMethyl)Morpholine
tert-butyl 2-(broMoMethyl)Morpholine-4-carboxylate
2-Bromomethylmorpholine-4-carboxylic acid tert-butyl ester
4-Morpholinecarboxylic acid, 2-(bromomethyl)-, 1,1-dimethylethyl ester
[Molecular Formula]

C10H18BrNO3
[MDL Number]

MFCD20489326
[MOL File]

765914-78-1.mol
[Molecular Weight]

280.16
Chemical PropertiesBack Directory
[Boiling point ]

328.8±32.0 °C(Predicted)
[density ]

1.334±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[pka]

-2.34±0.40(Predicted)
[Appearance]

White to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P260-P280-P301+P310
[HS Code ]

2934999090
Spectrum DetailBack Directory
[Spectrum Detail]

4-Boc-2-(broMoMethyl)Morpholine(765914-78-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-HYDROXYMETHYL-4-BOC-MORPHOLINE

135065-69-9

4-Boc-2-(broMoMethyl)Morpholine

765914-78-1

To a solution of tert-butyl 2-(hydroxymethyl)morpholine-4-carboxylate (0.67 g, 3.1 mmol) in dichloromethane (35 mL) was added carbon tetrabromide (CBr4, 2.06 g, 6.17 mmol) at -20 °C, followed by the slow dropwise addition of a solution of triphenylphosphine (PPh3, 1.70 g, 6.48 mmol) in dichloromethane (25 mL). The reaction mixture was maintained at -15 °C for 18 h, and subsequently brought to room temperature with continued stirring for 1.5 h. The reaction was carried out under reduced pressure. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure and the residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane) to afford the target product tert-butyl 2-(bromomethyl)morpholine-4-carboxylate 0.55 g in 63% yield, which was used directly in the subsequent reaction.

[References]

[1] Patent: WO2007/58850, 2007, A2. Location in patent: Page/Page column 44
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