Basic information Safety Supplier Related

1-Benzhydryl-3-iodoazetidine

Basic information Safety Supplier Related

1-Benzhydryl-3-iodoazetidine Basic information

Product Name:
1-Benzhydryl-3-iodoazetidine
Synonyms:
  • 1-Benzhydryl-3-iodoazetidine
  • N-Benzhydryl-3-iodoazetidine
  • Azetidine, 1-(diphenylMethyl)-3-iodo-
  • 3-Iodo-N-benzhydrylazetidine
  • 1-Diphenylmethyl-3-iodazo heterocyclic butane
  • 1-diphenylmethyl-3-iodoazacyclobutane
CAS:
125735-40-2
MF:
C16H16IN
MW:
349.21
Mol File:
125735-40-2.mol
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1-Benzhydryl-3-iodoazetidine Chemical Properties

Melting point:
101~102℃
Boiling point:
377℃
Density 
1.55
Flash point:
182℃
storage temp. 
2-8°C(protect from light)
pka
6.16±0.10(Predicted)
Appearance
White to yellow Solid
InChI
InChI=1S/C16H16IN/c17-15-11-18(12-15)16(13-7-3-1-4-8-13)14-9-5-2-6-10-14/h1-10,15-16H,11-12H2
InChIKey
IBCVAYQWXMWFLD-UHFFFAOYSA-N
SMILES
N1(C(C2=CC=CC=C2)C2=CC=CC=C2)CC(I)C1
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Safety Information

HS Code 
2933998090
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1-Benzhydryl-3-iodoazetidine Usage And Synthesis

Uses

1-Benzhydryl-3-iodoazetidine is a useful research reagent used in the synthetic preparation of other pharmacologically active molecules.

Synthesis

33301-41-6

125735-40-2

Step 1: Potassium iodide (530 mg, 3.14 mmol) was added to a mixed solution of 1-diphenylmethyl-3-methanesulfonic acid azetidine (500 mg, 1.57 mmol) in water (2.5 mL) and 1,2-dimethoxyethane (2.5 mL). The reaction mixture was stirred at room temperature and then heated to reflux and stirred continuously for 3 hours. After the reaction was completed, it was cooled to room temperature and diluted with water (50 mL) and ethyl acetate (50 mL). The aqueous phase was separated and extracted with ethyl acetate (2 x 70 mL). The organic phases were combined, washed with saturated sodium chloride solution (40 mL), dried over anhydrous sodium sulfate, filtered and concentrated to dryness to give 1-diphenylmethyl-3-iodoazetidine as a yellow solid (550 mg, 100% yield).LCMS (ESI-APCI) m/z 350.0 (M + H)+.

References

[1] Patent: WO2011/61214, 2011, A1. Location in patent: Page/Page column 159-160
[2] Patent: EP992493, 2000, A1
[3] Patent: EP962457, 1999, A1

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