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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2210301생성일: 2026년 10월 25일

N-methyl-2-pyrrolidone → tert-Butyl 2,4-dideoxy-3,5-O-(1-methylethylidene)-D-erythro-hexonate

https://huagongshe.com/reaction/2210301

반응식

참여 물질

역할이름HCID투입량
반응물N-methyl-2-pyrrolidoneHCID 13387—
반응물chloride (4R-cis)-6-(chloromethyl)-2,2-dimethyl-1,3-dioxane-4-acetic acid, 1,1-dimethylethyl esterHCID 86747487—
촉매Tetrabutylammonium AcetateHCID 82707—
생성물tert-Butyl 2,4-dideoxy-3,5-O-(1-methylethylidene)-D-erythro-hexonateHCID 9816650—

반응 조건

온도85 °C

반응 단계

Solid tetra-n-butylammonium acetate prepared in step (e)(i) of Example 1 above (106.2 g, 0.352 mole) was added in one portion to a mechanically stirred solution of the chloride (4R-cis)-6-(chloromethyl)-2,2-dimethyl-1,3-dioxane-4-acetic acid, 1,1-dimethylethyl ester prepared in step (d) of Example 1 above (32.7 g, 0.117 mole) in HPLC grade 1-methyl-2-pyrrolidinone (471 ml) under argon. The resulting solution was stirred at 85° C. (internal temperature). After 30 to 60 minutes the reaction mixture became homogeneous and brown in color. The progress of the reaction was followed by TLC and GC analysis. (TLC: Rf =0.54 for the title compound; Rf =0.63 for the chloride starting material (silica gel, Ethyl acetate:Hexane, 1:1, visualization by Ce(SO4)2 spray).) After 9 hours the reaction was completed.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05457227
출처 데이터셋uspto-grants-1995_10
ORD IDord-d2d09a3dd2ad41aaad1c3bbe051575ac
출처 메모uspto-grants-1995_10