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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944770Generated: October 31, 2026

Trifluoroacetic acid → (S)-2-Amino-3-(4-nitrophenyl)propan-1-ol

https://huagongshe.com/reaction/1944770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant(S)-2-(Boc-amino)-3-(4-nitrophenyl)-1-propanolHCID 12151763—
SolventDichloromethaneHCID 6344—
Product(S)-2-Amino-3-(4-nitrophenyl)propan-1-olHCID 10397777—

Reaction Steps

TFA (171 mL) was added to a solution of (S)-tert-butyl-1-hydroxy-3-(4-nitrophenyl)propan-2-ylcarbamate 20 (Erlanson et al., U.S. Pat. No. 7,214,487 B2; 13.9 g, 46.9 mmol) in DCM (272 mL) at 0° C. The reaction mixture was warmed to RT and reaction was allowed to proceed for 25 minutes. The solution was concentrated to afford 9.2 g of crude (S)-2-amino-3-(4-nitrophenyl)propan-1-ol as a white solid. To a solution of this crude product and sodium carbonate (12.4 g, 117.3 mmol) in THF (87 mL) and water (87 mL) was added N-carbethoxyphthalimide (“CEPT,” 12.3 g, 56.3 mmol). After the reaction mixture was stirred at RT for 4 h, EtOAc (150 mL) was added. The aqueous phase was extracted with EtOAc. The combined organic layers were washed with brine, dried over anhydrous Na2SO4, filtered and concentrated under vacuum to give a crude residue which was purified by flash chromatography eluting from silica gel with a gradient of 0-100% EtOAc in hexanes to give 12.3 g of alcohol 30. MS: (+) m/z 327.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394922B2
Source datasetuspto-grants-2013_03
ORD IDord-0df8d0153c1b444e82f9153018423bfe
Source noteuspto-grants-2013_03