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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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alpha5,alpha5-Dimethyl-3,5-isoxazoledimethanol → 5-(2-Hydroxypropan-2-yl)isoxazole-3-carbaldehyde

HRID 2261351
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HRID 2261351 반응식
[OH:1][C:2]([C:5]1[O:9][N:8]=[C:7]([CH2:10][OH:11])[CH:6]=1)([CH3:4])[CH3:3]>O1CCOCC1.[O-2].[O-2].[Mn+4]>[OH:1][C:2]([C:5]1[O:9][N:8]=[C:7]([CH:10]=[O:11])[CH:6]=1)([CH3:3])[CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 57736295alpha5,alpha5-Dimethyl-3,5-isoxazoledimethanol

생성물 1

HCID 451179925-(2-Hydroxypropan-2-yl)isoxazole-3-carbaldehyde수율 87.2%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 312751,4-Dioxane용매

실험 절차

5.38 g of [5-(1-hydroxy-1-methylethyl)isoxazol-3-yl]methanol was dissolved in 100 ml of 1,4-dioxane, and 29.74 g of manganese dioxide was then added. The mixture was stirred and heated under reflux for 10 hours. The reaction mixture was cooled to room temperature and then filtered through Celite®. The filtrate was concentrated under reduced pressure to obtain 4.63 g of 5-(1-hydroxy-1-methylethyl)-isoxazole-3-carbaldehyde.

후처리

  1. temperatureheated
  2. temperatureunder reflux for 10 hours
  3. filtrationfiltered through Celite®
  4. concentrationThe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-45d7122008ae4907b6071e5ce5ba8824
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07846956B2

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