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HRID 423049作成日:2026年10月25日

Methanol → 3-Amino-3-(4-chlorophenyl)propan-1-ol

https://huagongshe.com/reaction/423049

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物3-Amino-3-(4-chlorophenyl)propanoic acidHCID 344176—
溶媒TetrahydrofuranHCID 8028—
生成物3-Amino-3-(4-chlorophenyl)propan-1-olHCID 1703943556.8%

反応条件

温度0 °C

反応手順

Borane-tetrahydrofuran complex (94.0 mL, 93.92 mmol) was added dropwise to a stirred suspension of 3-amino-3-(4-chlorophenyl)propionic acid (2.50 g, 12.52 mmol) in THF (75 mL) at 0° C. over a period of 20 minutes under nitrogen. The resulting suspension was stirred at 0° C. for 30 minutes then at 22° C. for 5 hours. The reaction mixture was added portionwise to methanol (500 mL). The mixture was concentrated, redissolved in methanol (250 mL) and reconcentrated (this process was repeated three times). The residue was dissolved in DCM (200 mL) and washed with 1N NaOH (150 mL). The aqueous layer was extracted with DCM (5×100 mL) and the extracts combined with the organic layer. The combined organics were washed with saturated brine (2×150 mL), dried over MgSO4 and concentrated to afford a white semi-solid. The crude product was purified by flash silica chromatography, elution gradient 5 to 7% (10:1 MeOH/conc. NH3 (aq)) in DCM. Pure fractions were evaporated to dryness to afford 3-amino-3-(4-chlorophenyl)propan-1-ol (1.320 g, 56.8%) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08101623B2
出典データセットuspto-grants-2012_01
ORD IDord-86bbb29a1ac042cd89b6e1fee70c496a
出典メモuspto-grants-2012_01