Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68573생성일: 2026년 10월 24일
Methyl 5-formyl-2-methylfuran-3-carboxylate → 5-(1-Hydroxy-ethyl)-2-methyl-furan-3-carboxylic acid methyl ester
https://huagongshe.com/ko/reaction/68573
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Methyl 5-formyl-2-methylfuran-3-carboxylate | HCID 2779820 | — |
| 반응물 | HCID 178418573 | HCID 178418573 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-(1-Hydroxy-ethyl)-2-methyl-furan-3-carboxylic acid methyl ester | HCID 68292695 | — |
반응 단계
Methylmagnesium bromide (370.5 ml, 1.4M in THF) is added over 30 minutes to a solution of 5-formyl-2-methyl-furan-3-carboxylic acid methyl ester (87.2 g) in THF (1200 ml) under nitrogen at 0° C. After 1 hour at 0° C., the reaction is quenched with a saturated aqueous solution of NH4Cl in water. The mixture is stirred 1 hour at 0° C. and then is extracted three times with ethyl acetate. The organic phases are combined, dried over Na2SO4 and concentrated in verve to yield 5-(1-hydroxy-ethyl)-2-methyl-furan-3-carboxylic acid methyl ester (94.5 g) as a yellow solid. The crude product obtained is used without further purification. MS (HPLC/MS): 185 (MH+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08822466B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-b77cf627339442168587cf1cd4d38791 |
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| 출처 메모 | uspto-grants-2014_09 |
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