Trifluoroacetic acid → 3-((tert-Butyldimethylsilanyl)oxy)azetidine

HRID 500915Notes

Reaction equation

HRID 500915 reaction equation
[Si:1]([O:8][CH:9]1[CH2:12][N:11](C(OC(C)(C)C)=O)[CH2:10]1)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].C(O)(C(F)(F)F)=O>C(Cl)Cl>[Si:1]([O:8][CH:9]1[CH2:12][NH:11][CH2:10]1)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2]

Participants

4

Reactant 2

HCID 6422Trifluoroacetic acidHCID 59424599HCID 59424599, compound

Product 1

HCID 574386563-((tert-Butyldimethylsilanyl)oxy)azetidineYield 69%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

A mixture of 295 (200 mg, 0.696 mol), DCM (1 mL) and TFA (1 mL) was stirred for 1 h at room temperature, concentrated under reduced pressure; NaOH (1 M, 15 mL) was added to the residue and the suspension was extracted with DCM, the extract was dried (anhydrous Na2SO4) and concentrated, to afford title compound 296 (90.4 mg, 69% yield) as a syrup. MS (m/z): 188.1 (M+1).

Workup

  1. concentrationconcentrated under reduced pressure
  2. additionNaOH (1 M, 15 mL) was added to the residue
  3. extractionthe suspension was extracted with DCM
  4. dry with materialthe extract was dried (anhydrous Na2SO4)
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-ef299e39d1db439685d7798d197766c8
Source dataset
uspto-grants-2010_08
Patent number
US07772247B2

Reaction notes

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