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Water → 3-(3-Chloro-5-fluorophenyl)-1-ethylazetidin-3-ol

HRID 2041887
Notes
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Reaction equation

HRID 2041887 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:9]2([OH:13])[CH2:12][NH:11][CH2:10]2)[CH:5]=[C:6]([F:8])[CH:7]=1.C(=O)([O-])[O-].[K+].[K+].I[CH2:21][CH3:22].O>C(#N)C.C(OCC)(=O)C>[Cl:1][C:2]1[CH:3]=[C:4]([C:9]2([OH:13])[CH2:12][N:11]([CH2:21][CH3:22])[CH2:10]2)[CH:5]=[C:6]([F:8])[CH:7]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 962WaterHCID 6340IodoethaneHCID 11430Potassium CarbonateHCID 669953933-(3-Chloro-5-fluorophenyl)azetidin-3-ol

Product 1

HCID 462081073-(3-Chloro-5-fluorophenyl)-1-ethylazetidin-3-olYield 60.1%

Reagents, catalysts & solvents 2

HCID 6342
Acetonitrile
Solvent
HCID 8857Ethyl AcetateSolvent

Conditions

Temperature
120 °C

Procedure

A mixture of 3-(3-chloro-5-fluorophenyl)azetidin-3-ol (0.41 g, 2.03 mmol), potassium carbonate (0.56 g, 4.06 mmol) and iodoethane (0.31 g, 2.03 mmol) in acetonitrile (5 ml) was heated at 120° C. under microwave irradiation for 10 min. Water (50 ml) and ethyl acetate (50 ml) was added and the organic phase was collected. The aqueous phase was extracted with ethyl acetate (2×50 ml). The combined organic phase was dried (Na2SO4) and evaporated under reduced pressure to give the crude product. Purification by flash column chromatography on silica gel (ethyl acetate) gave 0.28 g (60%) of the title compound. The amine was converted to the fumaric acid salt and recrystallized from ethanol/diethyl ether/diisopropyl ether: M.p. 166-168° C. MS m/z (relative intensity, 70 eV) 229 (M+, 1), 172 (23), 130 (24), 109 (33), 58 (bp).

Workup

  1. customthe organic phase was collected
  2. extractionThe aqueous phase was extracted with ethyl acetate (2×50 ml)
  3. dry with materialThe combined organic phase was dried (Na2SO4)
  4. customevaporated under reduced pressure
  5. customto give the crude product
  6. customPurification by flash column chromatography on silica gel (ethyl acetate)

Sources & evidence

ORD record
ord-4652aae95b8240f3b3f5d251a489b02e
Source dataset
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08586572B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes