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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1168288생성일: 2026년 10월 27일

Oxalyl chloride → HCID 86585303, 화합물

https://huagongshe.com/reaction/1168288

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물DiisopropylethylamineHCID 81531—
반응물N-HydroxypropionimidamideHCID 4092053—
반응물ST092333HCID 10932896—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물HCID 86585303HCID 8658530388.2%

반응 단계

Oxalyl chloride (4 ml, 46 mmol) was added to a solution of (3aS,4S,6R,6aR)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole-4-carboxylic acid (Justus Liebigs Ann. Chem., 1974, 11, 1856) (5 g, 23 mmol) in dichloromethane (100 ml). The solution was stirred at room temperature for two hours and then the solvent was evaporated under reduced pressure to yield a white solid. This was dissolved in ethyl acetate (80 ml) and N′-hydroxypropanimidamide (2.63 g, 30 mmol) was added followed by N-ethyldiisopropylamine (8.12 ml, 46 mmol). The reaction mixture was stirred at room temperature for 48 hours and then washed with saturated sodium hydrogencarbonate solution (50 ml) and brine (50 ml). The organic layer was separated, dried (anhydrous magnesium sulphate) and evaporated under reduced pressure to give the product as a dark yellow oil (5.85 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06624158B2
출처 데이터셋uspto-grants-2003_09
ORD IDord-e098c59da3e64362a248b7f904bf4b62
출처 메모uspto-grants-2003_09