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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1471307생성일: 2026년 10월 25일

Triethylamine → (2-{2-[2-((2R,3R,4R,5R,6R)-4,5-Diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-2-yloxy)-ethoxy]-ethoxy}-ethoxy)-acetic acid benzyl ester

https://huagongshe.com/reaction/1471307

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Trimethylsilyl triflateHCID 65367—
반응물(3aR,5R,6R,7R,7aR)-5-(acetoxymethyl)-2-methyl-5,6,7,7a-tetrahydro-3aH-pyrano[3,2-d]oxazole-6,7-diyl diacetateHCID 11278902—
반응물Benzyl 2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)acetateHCID 58409191—
용매DichloromethaneHCID 6344—
생성물(2-{2-[2-((2R,3R,4R,5R,6R)-4,5-Diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-2-yloxy)-ethoxy]-ethoxy}-ethoxy)-acetic acid benzyl esterHCID 5840919596.2%

반응 단계

The above prepared acetic acid (3aR,5R,6R,7R,7aR)-6-acetoxy-5-acetoxymethyl-2-methyl-5,6,7,7a-tetrahydro-3aH-pyrano[3,2-d]oxazol-7-yl ester (10.3 g, 26 mmol) and {2-[2-(2-hydroxy-ethoxy)-ethoxy]-ethoxy}-acetic acid benzyl ester (8.62 g, 29 mmol) were mixed in 520 mL of CH2Cl2 and treated with 63 g of 4 Angstrom molecular sieves. After 1 h trimethylsilyl triflate (6.13 g, 28 mmol) was added. The reaction mixture was stirred over the weekend at ambient temperature. Triethylamine (5.21 ml, 37 mmol) was added, the molecular sieves filtered off, the filtrate diluted with CH2Cl2 and washed with NaHCO3-solution and water. Drying over Na2SO4 and evaporation of the solvent followed by flash chromatography (SiO2, ethyl acetate/AcOH/MeOH/water=60/3/3/2) afforded 15.7 g of the title compound as a brownish oil. MS (ISP): 626.6 [M−H]−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09011919B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-b051286d171d4436a912b10bbe4aba2c
출처 메모uspto-grants-2015_04