Trifluoroacetic acid methylene chloride → HCID 86619130, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:18])[C@H:4]([CH2:13][C:14]([CH3:17])([CH3:16])[CH3:15])[NH:5]C(OC(C)(C)C)=O.[C:19]([OH:25])([C:21]([F:24])([F:23])[F:22])=[O:20].ClCCl>>[F:22][C:21]([F:24])([F:23])[C:19]([OH:25])=[O:20].[CH3:1][O:2][C:3](=[O:18])[C@H:4]([CH2:13][C:14]([CH3:16])([CH3:15])[CH3:17])[NH2:5]Participants
3
Procedure
The (2S)—N-tert-butoxycarbonyl-3-tert-butyl-L-alanine methyl ester (529 mg, 2.04 mmol) is stirred at RT in TFA/dichloromethane 1:3 (3 ml), and the solution is concentrated on a rotary evaporator and dried under high vacuum. 540 mg (97% of theory) of product are obtained.
Workup
- concentrationthe solution is concentrated on a rotary evaporator
- customdried under high vacuum
- custom540 mg (97% of theory) of product are obtained
Sources & evidence
- ORD record
- ord-31d57d1a62364e709a624f6c6dd597a3
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07718611B2
Reaction notes
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