Basic information Safety Supplier Related

METHYL 1-(DIPHENYLMETHYL)AZETIDINE-3-CARBOXYLATE

Basic information Safety Supplier Related

METHYL 1-(DIPHENYLMETHYL)AZETIDINE-3-CARBOXYLATE Basic information

Product Name:
METHYL 1-(DIPHENYLMETHYL)AZETIDINE-3-CARBOXYLATE
Synonyms:
  • 1-BENZHYDRYL-AZETIDINE-3-CARBOXYLIC ACID METHYL ESTER
  • METHYL 1-(DIPHENYLMETHYL)AZETIDINE-3-CARBOXYLATE
  • BUTTPARK 37\04-18
  • METHYL 1-BENZHYDRYLAZETIDINE-3-CARBOXYLATE
  • N-BENZHYDRYLAZETIDINE-3-CARBOXYLIC ACID METHYL ESTER
  • Methyl 1-diphenylMethyl-a...
  • Methyl 1-benzhydrylazetidine-3-carboxylate, Methyl 1-benzhydrylazetane-3-carboxylate
  • 1-(Diphenylmethyl)azetidine-3-carboxylic acid methyl ester
CAS:
53871-06-0
MF:
C18H19NO2
MW:
281.35
Mol File:
53871-06-0.mol
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METHYL 1-(DIPHENYLMETHYL)AZETIDINE-3-CARBOXYLATE Chemical Properties

Melting point:
67-70°C
Boiling point:
366℃
Density 
1.163
Flash point:
122℃
storage temp. 
Sealed in dry,Room Temperature
pka
6.41±0.10(Predicted)
Appearance
White to light brown Solid
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Safety Information

HS Code 
2933998090
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METHYL 1-(DIPHENYLMETHYL)AZETIDINE-3-CARBOXYLATE Usage And Synthesis

Synthesis

36476-87-6

74-88-4

53871-06-0

GENERAL STEPS: Potassium carbonate (6.53 g, 47.2 mmol) and iodomethane (0.976 mL, 15.7 mmol) were sequentially added to a solution of N,N-dimethylformamide (45 mL) of 1-diphenylmethylazetidine-3-carboxylic acid (4.20 g, 15.7 mmol) and the reaction was stirred at room temperature for 20.5 hours. After completion of the reaction, the reaction mixture was slowly poured into ice water and extracted with ethyl acetate (3 × 50 mL). The organic layers were combined, washed with saturated saline (50 mL) and dried over anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure and the resulting crude product was purified by silica gel column chromatography (elution gradient: heptane/ethyl acetate = 5:1 to 3:1). The fraction containing the target compound was collected and concentrated under reduced pressure to give methyl 1-diphenylmethylazetidine-3-carboxylate (3.57 g, 80.8% yield) as yellow crystals.1H NMR (400 MHz, CDCl3) δ: 3.26 (m, 2H), 3.31 (m, 1H), 3.44 (m, 2H), 3.69 (s, 3H), 4.38 (s, 1H), 7.16-7.16-7.16 1H), 7.16-7.20 (m, 2H), 7.25-7.28 (m, 4H), 7.39-7.41 (m, 4H). ESI-MS m/z: 282 [M + H]+.

References

[1] Patent: US2008/214815, 2008, A1. Location in patent: Page/Page column 14
[2] Patent: EP1889836, 2008, A1. Location in patent: Page/Page column 80

METHYL 1-(DIPHENYLMETHYL)AZETIDINE-3-CARBOXYLATESupplier

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