Trifluoroacetic acid → HCID 59200381, compound
Reaction equation
[CH2:1]([NH:6][CH2:7][C:8]([C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[CH2:9][NH:10]C(=O)OC(C)(C)C)[C:2]([CH3:5])([CH3:4])[CH3:3].FC(F)(F)C(O)=O>ClCCl>[CH2:1]([NH:6][CH2:7][C:8]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)([C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)[CH2:9][NH2:10])[C:2]([CH3:5])([CH3:4])[CH3:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title material was prepared by treating a solution of the crude tert-butyl 3-(neopentylamino)-2,2-diphenylpropylcarbamate (0.055 g) in dichloromethane (5 mL) with trifluoroacetic acid (1 mL) at 23° C. for 30 minutes. The reaction was concentrated to dryness and the residue was used as such in the next reaction.
Workup
- concentrationThe reaction was concentrated to dryness
- customsuch in the next reaction
Sources & evidence
- ORD record
- ord-c61c9d3128a24100bc6d251d548273ad
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08148400B2
Reaction notes
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