戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 726655作成日:2026年10月26日

2,4,5-Trichlorophenol → Cbz-D-hPro-Pro-OH

https://huagongshe.com/reaction/726655

反応式

関与物質

役割名称HCID仕込み量
反応物2,4,5-TrichlorophenolHCID 7271—
反応物TriethylamineHCID 8471—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物L-ProlineHCID 145742—
反応物(2R)-1-((Benzyloxy)carbonyl)piperidine-2-carboxylic acidHCID 688346—
溶媒Ethyl AcetateHCID 8857—
生成物Cbz-D-hPro-Pro-OHHCID 22854903—

反応条件

温度0 °C

反応手順

Cbz-D-hPro-OH (9.5 g, 36 mmol) was dissolved in ethyl acetate (100 mL) and the solution cooled to 0° C. Added to the solution was 2,4,5-trichlorophenol (7.1 g, 36 mmol) and 1,3-dicyclohexylcarbodiimide (7.4 g, 36 mmol). The reaction was stirred for 1 hour at 0° C. and 1 hour at room temperature. The precipitate was filtered and the filtrate concentrated in vacuo to an oil. The oil was dissolved in pyridine (100 mL), Pro-OH (4.2 g, 36 mmol), and triethylamine (5.0 mL, 36 mmol) were added. The reaction was stirred at room temperature (24 hours). The reaction solvent was removed in vacuo to an oil. The residue was dissolved in water (100 mL), diethyl ether (50 mL) was added and the pH adjusted to 9.5 with 2N sodium hydroxide. The aqueous layer extracted twice with diethyl ether. The aqueous layer separated, the pH adjusted to 2.8 with 3N hydrochloric acid and ethyl acetate (150 mL) was added. The organic layer was separated, dried (MgSO4), and the filtrate evaporated in vacuo to an amorphous solid (11.4 g, 88%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05710130
出典データセットuspto-grants-1998_01
ORD IDord-4f15455e5bda4e229be67e140928d4fb
出典メモuspto-grants-1998_01