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1-(Diphenylmethyl)-3-Hydroxyazetidine Hydrochloride

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1-(Diphenylmethyl)-3-Hydroxyazetidine Hydrochloride Basic information

Product Name:
1-(Diphenylmethyl)-3-Hydroxyazetidine Hydrochloride
Synonyms:
  • N-BENZHYDRYLAZETIDIN-3-OL HCL
  • 1-BENZHYDRYL AZETIDIN-3-OL HCL
  • 1-BENZHYDRYLAZETIDIN-3-OL HYDROCHLORIDE
  • 1-(DIPHENYLMETHYL)-3-HYDROXYAZETIDINE HYDROCHLORIDE
  • 1-(Diphenylmethyl)-3-azetidinolhydrochloride
  • 1-Benzhydrylazetidin-3-ol hydrochloride 95%
  • 3-Azetidinol, 1-(diphenylMethyl)-, hydrochloride
  • 1-Benzhydrazylazetidin-3-ol hydrochloride
CAS:
90604-02-7
MF:
C16H18ClNO
MW:
275.78
Mol File:
90604-02-7.mol
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1-(Diphenylmethyl)-3-Hydroxyazetidine Hydrochloride Chemical Properties

Melting point:
172-174°C
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Chloroform (Slightly, Heated, Sonicated), DMSO (Slightly, Heated), Methanol (Slightly)
form 
Solid
color 
White to Pale Yellow
CAS DataBase Reference
90604-02-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37
Hazard Note 
Irritant
HS Code 
2934999090
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1-(Diphenylmethyl)-3-Hydroxyazetidine Hydrochloride Usage And Synthesis

Uses

1-(Diphenylmethyl)-3-Hydroxyazetidine Hydrochloride is a vital compound and can be used to synthesise 1-Benzhydrylazetidin-3-one and 1-benzhydrylazetidin-3-ol.

Synthesis

18621-17-5

90604-02-7

General procedure for the synthesis of 1-(diphenylmethyl)-3-hydroxyazetidine hydrochloride from 1-diphenylmethyl-3-hydroxyazetidine: 1-(diphenylmethyl)-3-hydroxyazetidine (9.70 g) was suspended in a 4.5 M hydrochloric acid solution of ethyl acetate (35 mL) at room temperature and the reaction was stirred for 10 minutes. Subsequently, the solvent was removed by evaporation to give 1-(diphenylmethyl)-3-hydroxyazetidine hydrochloride (12.0 g, 100% yield). The product was characterized by 1H-NMR (300 MHz, DMSO-d6, with TMS as internal standard) with the following chemical shifts (ppm): δ 7.30-7.70 (10H, m, arylhydrogen), 5.85 (1H, s, CH), 5.80 (1H, d, OH), 4.46 (1H, m, CH), 3.70-4.20 (4H, m, CH2 ).

References

[1] Patent: WO2007/118830, 2007, A1. Location in patent: Page/Page column 91

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