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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 726655생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/726655

반응식

참여 물질

역할이름HCID투입량
반응물2,4,5-TrichlorophenolHCID 7271—
반응물TriethylamineHCID 8471—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물L-ProlineHCID 145742—
반응물(2R)-1-((Benzyloxy)carbonyl)piperidine-2-carboxylic acidHCID 688346—
용매Ethyl AcetateHCID 8857—
생성물Cbz-D-hPro-Pro-OHHCID 22854903—

반응 조건

온도0 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05710130
출처 데이터셋uspto-grants-1998_01
ORD IDord-4f15455e5bda4e229be67e140928d4fb
출처 메모uspto-grants-1998_01