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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 747800생성일: 2026년 10월 25일

Methanol → Methyl 3-azido-2-hydroxypropionate

https://huagongshe.com/reaction/747800

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Sodium CarbonateHCID 10340—
반응물Methanesulfonyl azide, trifluoro-HCID 10986786—
반응물Methyl 3-amino-2-hydroxypropanoate hydrochlorideHCID 71757671—
촉매Copper SulfateHCID 24462—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물Methyl 3-azido-2-hydroxypropionateHCID 1015411657%

반응 단계

To an ice-cold mixture of methyl 3-amino-2-hydroxypropionate hydrochloride (19) (27.1 g, 0.17 mol) in water (100 mL) and dichloromethane (100 mL) was added sodium carbonate (19.82 g, 0.187 mol) and CuSO4. 5H2O (0.3 g, 1.2 mmol) with stirring. Triflylazide from experiment 10(B)(i) (crude, 44.6 g, 0.25 mol) was added dropwise keeping the reaction temperature at 0-5° C. Methanol (about 100 mL) was added until the reaction mixture became homogeneous. The reaction mixture was allowed to come to room temperature and then stirred for 20 h. Water (500 mL) was added and the aqueous solution thoroughly extracted with dichloromethane (5×100 mL). The combined organic layers were washed with water (2×200 mL), saturated sodium carbonate (2×200 mL), and then dried (anhydrous sodium sulfate). After removal of the solvent, the residue was chromatographed over silica gel. Elution with 30% ethyl acetate in hexanes furnished the product as a colorless oil (14.0 g; Yield: 57%) Rf 0.57 (30% ethyl acetate in hexanes).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07399460B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-7c25f9a433a94596837ca08a72d607fe
출처 메모uspto-grants-2008_07