Trifluoroacetic acid → HCID 58606959, compound
Reaction equation
[CH2:1]([NH:11][C:12]([C@@H:14]1[CH2:17][CH2:16][N:15]1C(OC(C)(C)C)=O)=[O:13])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].FC(F)(F)C(O)=O>C(Cl)Cl>[CH2:1]([NH:11][C:12]([C@@H:14]1[CH2:17][CH2:16][NH:15]1)=[O:13])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
N-(tert-Butoxycarbonyl)-(S)-(−)-2-azetidinecarboxylic acid n-decyl amide (285) (160 mg; 0.470 mmol) is dissolved in methylene chloride (4 mL) at ambient temperature. Trifluoroacetic acid (2 mL) is added and the solution is stirred for 2 hours at ambient temperature. The solution is concentrated in vacuo at 40° C. The residue is dissolved in methylene chloride (20 mL) and poured onto saturated sodium bicarbonate solution. The pH is adjusted to 9 with saturated potassium carbonate solution. The mixture is shaken and the layers separated. The water layer is extracted with methylene chloride (3 times, 5 mL each). The combined organic extracts are washed with water, dried over MgSO4, filtered, and concentrated in vacuo affording the desired product (289) as a solid. ISMS: MH+ 241.2
Workup
- concentrationThe solution is concentrated in vacuo at 40° C
- dissolutionThe residue is dissolved in methylene chloride (20 mL)
- additionpoured onto saturated sodium bicarbonate solution
- stirringThe mixture is shaken
- customthe layers separated
- extractionThe water layer is extracted with methylene chloride (3 times, 5 mL each)
- washThe combined organic extracts are washed with water
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-cc64ce620c6e4be797f14e3f319bbceb
- Source dataset
- uspto-grants-2006_03
- Patent number
- US07018642B2
Reaction notes
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