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135072-15-0

135072-15-0 Structure

135072-15-0 Structure
IdentificationBack Directory
[Name]

4-BENZYL-2-MORPHOLINECARBOXYLIC ACID HYDROCHLORIDE
[CAS]

135072-15-0
[Synonyms]

135072-15-0
4-Benzyl-2-morpholinecarboxylicacidHCl
4-Benzyl-2-carboxymorpholine hydrochloride
BENZYL(N-)-MORPHOLINE-2-CARBOXYLIC ACID HCL
4-BENZYL-2-MORPHOLINECARBOXYLIC ACID HYDROCHLORIDE
4-BENZYL-MORPHOLINE-2-CARBOXYLIC ACID HYDROCHLORIDE
4-Benzylmorpholine-2-carboxylicacidhydrochloride,97%
4-Benzyl-2-morpholinecarboxylic acid hydrochloride, 90+%
2-Morpholinecarboxylic acid, 4-(phenylmethyl)-, hydrochloride
[Molecular Formula]

C12H16ClNO3
[MDL Number]

MFCD02682031
[MOL File]

135072-15-0.mol
[Molecular Weight]

257.71
Chemical PropertiesBack Directory
[Melting point ]

244 °C
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

solid
[color ]

Brown
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

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

P261-P280-P304+P340-P305+P351+P338-P405-P501a
[Hazard Codes ]

Xn
[Risk Statements ]

36/37/38-20/21/22
[Safety Statements ]

26-36/37/39
[Hazard Note ]

Harmful
[HazardClass ]

6.1
[HS Code ]

2934999090
Spectrum DetailBack Directory
[Spectrum Detail]

4-BENZYL-2-MORPHOLINECARBOXYLIC ACID HYDROCHLORIDE(135072-15-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-benzylmorpholine-2-carbonitrile

147767-51-9

4-BENZYL-2-MORPHOLINECARBOXYLIC ACID HYDROCHLORIDE

135072-15-0

4-Benzylmorpholine-2-carbonitrile (64.1 g, 316.9 mmol) was used as the raw material, which was dissolved in 6 N aqueous hydrochloric acid (600 mL) and the reaction was heated to reflux for 2.5 hours. After the reaction was completed, the reaction solution was cooled to -10 °C. The precipitated solid product was collected by filtration and washed with acetone (300 mL) pre-cooled to -10 °C. The resulting solid was dried in an oven at 60 °C to afford 4-benzyl-2-morpholine carboxylic acid hydrochloride (78.7 g, 305.4 mmol, 96% yield). The product was characterized by 1H NMR (400 MHz, DMSO-d6): δ 2.18 (broad peak, -COOH), 7.67-7.65 (multiple peaks, 2H), 7.53-7.40 (multiple peaks, 3H), 4.61 (double peak, J = 10.8 Hz, 1H), 4.39 (multiple peaks, 2H), 4.05-4.94 (multiple peaks, 2H) , 3.43 (double peak, J = 12.0 Hz, 1H), 3.20-3.07 (multiple peaks, 3H).

[References]

[1] Patent: WO2012/128582, 2012, A2. Location in patent: Page/Page column 28
[2] Patent: WO2005/47272, 2005, A1. Location in patent: Page/Page column 48-49
[3] Organic Process Research and Development, 2009, vol. 13, # 2, p. 209 - 224
[4] Patent: WO2010/59658, 2010, A1. Location in patent: Page/Page column 225
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