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HRID 1671394作成日:2026年10月27日

Hydrochloric Acid → (S)-3-[1-(2,3,6-Trichlorophenoxy)prop-2-ynyl]pyrrolidine

https://huagongshe.com/reaction/1671394

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物EthanolHCID 702—
反応物PhenolHCID 996—
反応物TriphenylphosphineHCID 11776—
反応物2,3,6-TrichlorophenolHCID 13618—
反応物Diisopropyl azodicarboxylateHCID 5363146—
反応物(S)-3-(1-Hydroxyprop-2-ynyl)pyrrolidine-1-carboxylic Acid t-Butyl EsterHCID 58104606—
溶媒TolueneHCID 1140—
生成物(S)-3-[1-(2,3,6-Trichlorophenoxy)prop-2-ynyl]pyrrolidineHCID 58104602—

反応条件

温度100 °C

反応手順

A mixture of (S)-3-(1-hydroxyprop-2-ynyl)pyrrolidine-1-carboxylic acid t-butyl ester (21.0 mg, 93.2 μmmol) and DIAD (22.0 μL, 112 μmmol) was dissolved in toluene (65 μL, 610 μmmol) at room temperature. PPh3 (29.3 mg, 112 μmmol) and 2,3,6-trichlorophenol (20.2 mg, 102 μmmol) were dissolved in toluene (0.1 mL, 1 mmol) and heated at 100° C. The t-butyl ester mixture was slowly added into the phenol mixture at 100° C., and stirred for 1 hour. The mixture was then removed from the heat and stirred at room temperature overnight. The mixture was then concentrated and the resulting residue was treated with 1.25M HCl in EtOH (0.6 mL, 0.8 mmol) at room temperature overnight. The mixture was concentrated and the residue was redissolved in a mixture of 50% AcOH/H2O (1.4 mL) and MeCN (0.2 mL), filtered and purified by reverse phase preparative HPLC to yield the title compound as a mono-TFA salt (21.2 mg, 99% purity). MS m/z: [M+H]+ calcd for C13H12Cl3NO, 304.00; found 304.0.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07994209B2
出典データセットuspto-grants-2011_08
ORD IDord-8d4c5d4177814026bd8e1e6398f39400
出典メモuspto-grants-2011_08