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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595800Generated: November 1, 2026

(2S)-(Methylamino)(phenyl)acetic acid → (S)-2-(Methylamino)-2-phenylethanol

https://huagongshe.com/reaction/595800

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S)-(Methylamino)(phenyl)acetic acidHCID 681675—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(S)-2-(Methylamino)-2-phenylethanolHCID 1005768755%

Reaction Steps

To a suspension of LiAlH4 (0.689 g, 18.16 mmol) in THF (20.18 mL) was added (S)-2-(methylamino)-2-phenylacetic acid (1 g, 6.05 mmol) in THF (20 mL) slowly over 10 min at 0° C. The reaction mixture was stirred at room temperature for overnight. After quenched with water (0.7 mL), NaOH (2.1 mL), water (0.7 mL). The reaction mixture was filtered off. The filtrate was extracted with EtOAc 3 times. The combined organic layer was washed with water and brine, dried over anhydrous sodium sulfate, filtered off, and concentrated in vacuo. The crude product was purified by flash chromatography (10% methanol in DCM) yielding (S)-2-(methylamino)-2-phenylethanol as a colorless oil in 55% yield. LCMS (m/z): 152.1 (MH+), 0.31 min; 1H NMR (400 MHz, CDCl3) δ7.40-7.33 (m, 2H), 7.32-7.27 (m, 3H), 3.77-3.69 (m, 1H), 3.69-3.63 (m, 1H), 3.58 (d, J=9.8 Hz, 1H), 2.36 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-90b51c5f4bee437b9b88568f646d8b79
Source noteuspto-grants-2016_01