Basic information Safety Supplier Related

(S)-4-BENZYL-3-CHLOROMETHYL-MORPHOLINE

Basic information Safety Supplier Related

(S)-4-BENZYL-3-CHLOROMETHYL-MORPHOLINE Basic information

Product Name:
(S)-4-BENZYL-3-CHLOROMETHYL-MORPHOLINE
Synonyms:
  • Morpholine, 3-(chloroMethyl)-4-(phenylMethyl)-, (3S)-
  • (S)-4-BENZYL-3-CHLOROMETHYL-MORPHOLINE
  • (3S)-4-benzyl-3-(chloromethyl)morpholine
CAS:
917572-28-2
MF:
C12H16ClNO
MW:
225.71
Mol File:
917572-28-2.mol
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(S)-4-BENZYL-3-CHLOROMETHYL-MORPHOLINE Chemical Properties

Boiling point:
316.1±27.0 °C(Predicted)
Density 
1.132±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
5.53±0.40(Predicted)
Appearance
Colorless to light yellow Liquid
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(S)-4-BENZYL-3-CHLOROMETHYL-MORPHOLINE Usage And Synthesis

Synthesis

101376-26-5

917572-28-2

(a) Synthesis of (3S)-4-benzyl-3-(chloromethyl)morpholine: [(3R)-4-benzylmorpholin-3-yl]methanol (1.83 g, 8.8 mmol) was dissolved in anhydrous dichloromethane (15 mL) under argon protection. To this solution thionyl chloride (3.15 g, 26.5 mmol) and N,N-dimethylformamide (DMF, 2 drops) were added sequentially. The reaction mixture was heated to reflux with continuous stirring for 2 h 30 min. After completion of the reaction, the solvent was removed by rotary evaporator. The residue was neutralized with saturated aqueous sodium bicarbonate and subsequently extracted with ethyl acetate (3 × 15 mL). The organic phases were combined, dried with anhydrous sodium sulfate, filtered and concentrated to afford the oily product (3S)-4-benzyl-3-(chloromethyl)morpholine (1.88 g, 94% yield). The product was characterized by 1H NMR (500 MHz, CDCl3) and LCMS: 1H NMR (500 MHz, CDCl3) δ 2.3-2.4 (m, 1H), 2.7 (m, 1H), 2.8 (m, 1H), 3.5 (d, 1H), 3.6-3.9 (m, 5H), 4.0 (d, 1H), 7.3 (m, 1H) , 7.4 (m, 4H); LCMS: m/z 226 [M + H]+.

References

[1] Patent: WO2006/137790, 2006, A1. Location in patent: Page/Page column 32
[2] Patent: WO2006/137791, 2006, A1. Location in patent: Page/Page column 43
[3] Patent: WO2011/111875, 2011, A1. Location in patent: Page/Page column 90
[4] Journal of Medicinal Chemistry, 2017, vol. 60, # 6, p. 2227 - 2244

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