ChemicalBook--->CAS DataBase List--->921609-34-9

921609-34-9

921609-34-9 Structure

921609-34-9 Structure
IdentificationBack Directory
[Name]

(S)-2-Amino-3-(4-(trifluoromethoxy)phenyl)propanoic acid hydrochloride
[CAS]

921609-34-9
[Synonyms]

(S)-2-AMINO-3-(4-(TRIFLUOROMETHOXY)PHENYL)PROPANOIC ACID HCL
(S)-2-Amino-3-(4-(trifluoromethoxy)phenyl)propanoic acid hydrochloride
(2S)-2-AMINO-3-[4-(TRIFLUOROMETHOXY)PHENYL]PROPANOIC ACID HYDROCHLRIDE
[Molecular Formula]

C10H11ClF3NO3
[MDL Number]

MFCD28986154
[MOL File]

921609-34-9.mol
[Molecular Weight]

285.65
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

(S)-2-Amino-3-(4-(trifluoromethoxy)phenyl)propanoic acid hydrochloride(921609-34-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

L-Tyrosine, N-acetyl-O-(trifluoromethyl)-, methyl ester

921623-42-9

(S)-2-Amino-3-(4-(trifluoromethoxy)phenyl)propanoic acid hydrochloride

921609-34-9

General procedure for the synthesis of (S)-2-amino-3-(4-(trifluoromethoxy)phenyl)propanoic acid hydrochloride from the compound (CAS: 921623-42-9): methyl (2S)-2-(acetylamino)-3-[4-(trifluoromethoxy)phenyl]propanoate (29.9 mg, 0.098 mmol) prepared in Reference Example 3 was mixed with 6 N hydrochloric acid ( 330 μL) were mixed and the reaction was stirred at 100 °C for 4 hours. Upon completion of the reaction, the reaction solution was cooled to room temperature and subsequently concentrated under reduced pressure. The resulting residue was azeotroped with toluene, washed with ether and dried under reduced pressure to give 26 mg (S)-2-amino-3-(4-(trifluoromethoxy)phenyl)propionic acid hydrochloride (white powder, yield: 93%).

[References]

[1] Patent: EP1908466, 2008, A1. Location in patent: Page/Page column 121
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