Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 867976생성일: 2026년 10월 24일
Tetrahydrofuran → (3R,6S)-3-isopropyl-6-(2-(3-methylpropoxymethylphosphoryl)ethyl)-2,5-dimethoxy-3,6-dihydropyrazine
https://huagongshe.com/ko/reaction/867976
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | (R)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine | HCID 736066 | — |
| 반응물 | 2-Methylpropyl (2-chloroethyl)methylphosphinate | HCID 13853109 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | (3R,6S)-3-isopropyl-6-(2-(3-methylpropoxymethylphosphoryl)ethyl)-2,5-dimethoxy-3,6-dihydropyrazine | HCID 86742474 | — |
반응 단계
5.53 g (0.03 mol) of (3R)-(-)-3-isopropyl-2,5-dimethoxy-3,6-dihydropyrazine ([α]D25 =-107.5°, c=1 in ethanol) are dissolved in 50 ml of absolute tetrahydrofuran, and 20.6 ml of a 1.6-molar solution of n-butyllithium in n-hexane are added at -75° C. The reaction mixture is stirred at -75° C. for 15 minutes. A solution, previously cooled to -60° C., of 6.1 g (0.031 mol) of 2-methylpropyl 2-chloroethyl(methyl)phosphinate in 30 ml of tetrahydrofuran is added dropwise in the course of 7 minutes at -75° C. The reaction mixture is stirred for 6 hours at -75° C. and then for 14 hours at room temperature. The solvent is removed completely in vacuo and the residue is taken up in 60 ml of diethyl ether. This solution is extracted once with 60 ml of water and once with 30 ml of saturated sodium chloride solution. The organic phase is dried over MgSO4 and completely freed from solvents. The residue is distilled in a high vacuum. This gives 8.84 g (85.1% of theory) of (3R,6S)-3-isopropyl-6-[2-(3-methylpropoxymethylphosphoryl)ethyl]-2,5-dimethoxy-3,6-dihydropyrazine as a low-melting solid of boiling point 155°-162° C./0.001 bar.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04777279 |
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| 출처 데이터셋 | uspto-grants-1988_10 |
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| ORD ID | ord-05694cb060a349e8b6275e79ee3f1cb8 |
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| 출처 메모 | uspto-grants-1988_10 |
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