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
Participants
| Role | Name | HCID | Charge |
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| Reactant | (2S)-(Methylamino)(phenyl)acetic acid | HCID 681675 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-2-(Methylamino)-2-phenylethanol | HCID 10057687 | 55% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242996B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-90b51c5f4bee437b9b88568f646d8b79 |
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| Source note | uspto-grants-2016_01 |
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