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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351471Generated: November 1, 2026

Sodium Hydroxide → (1S)-1-phenyl-2-(phenylamino)ethan-1-ol

https://huagongshe.com/reaction/1351471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantN-(2-phenyl-2-(S)-hydroxyethyl)-4-(2-aminoethyl)aniline trifluoroacetateHCID 22986855—
SolventMethanolHCID 887—
Product(1S)-1-phenyl-2-(phenylamino)ethan-1-olHCID 39243263—

Reaction Steps

To a solution of N-(2-phenyl-2-(S)-hydroxyethyl)-4-(2-aminoethyl)aniline trifluoroacetate 31 (0.144 g, 0.3 mmole) in methanol (10 mL) was added aq. NaOH solution (1.0 M, 0.625 mL). The solution was concentrated to dryness and the residue was dissolved in anhydrous THF (5 mL). α,α-Dihydroxy-4-hydroxy-3-methoxycarbonylacetophenone 12 (0.067 g, 0.3 mmole) was added and the reaction mixture was stirred for 12 h at rt. BH3-Me2S (0.2 mL, 2M) was added at 0° C. and the reaction mixture was heated at 75° C. for 6 h. After cooling the reaction mixture in ice bath, MeOH (5 mL) was slowly added to it to quench the reaction, and the reaction mixture was stirred for 30 min., at rt. The organics were removed and the residue was dissolved in TFA/MeOH (1/9; 20 mL), and concentrated. The crude product was dissolved in 20% MeCN/H2O, and purified by preparative HPLC: 5 to 20% MeCN/H2O; 20 mL/min; 254 nm.) to give 1-{2-[N-2-(4-hydroxy-3-hydroxy-methylphenyl)-2-hydroxyethyl]amino]ethyl}-4-[N-(2-phenyl-2-(S)-hydroxyethyl)-amino]benzene 33.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217738B2
Source datasetuspto-grants-2007_05
ORD IDord-c265b2afde6040c78a21c59163b48527
Source noteuspto-grants-2007_05