Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16341생성일: 2026년 10월 24일
Hydrogen Peroxide → (S)-4-[(S)-1-(2,6-difluoropyridin-3-yl)ethyl]-2-hydroxy-6-methylmorpholin-3-one
https://huagongshe.com/ko/reaction/16341
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrogen Peroxide | HCID 784 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Lithium tri-s-butylborohydride | HCID 3611392 | — |
| 반응물 | Sodium Bisulfite | HCID 23665763 | — |
| 반응물 | (S)-4-[(S)-1-(2,6-difluoropyridin-3-yl)ethyl]-6-methylmorpholine-2,3-dione | HCID 68717775 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Tetrahydrofuran toluene | HCID 22635083 | — |
| 생성물 | (S)-4-[(S)-1-(2,6-difluoropyridin-3-yl)ethyl]-2-hydroxy-6-methylmorpholin-3-one | HCID 68717852 | 99.7% |
반응 단계
A THF solution (20 mL) of 1 M lithium tri-s-butyl borohydride was dropwise added to a THF solution of (S)-4-[(S)-1-(2,6-difluoropyridin-3-yl)ethyl]-6-methylmorpholin-2,3-dione (4.5 g) at −50° C. or below. The resulting reaction solution was stirred for 2 hr. To the reaction solution, a 5 N sodium hydroxide aqueous solution (1.66 mL) and 30% hydrogen peroxide aqueous solution (6.78 mL) were added in this order at −10° C. or below. The resulting reaction solution was stirred for 1 hr, and then sodium hydrogensulfite (520 mg) was added thereto. The resulting reaction solution was stirred for 30 min, and then saturated saline and 50% toluene-THF were added thereto. The organic layer was separated, and the water layer was extracted with 50% toluene-THF. All the organic layers were combined and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (heptane:ethyl acetate=1:1 to 0:1) to give 4.52 g of the title compound. The physical property values of this compound were as follows:
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07737141B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-e4add3c7b0cb46f892e2e022b2640d7e |
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| 출처 메모 | uspto-grants-2010_06 |
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