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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Formamidine acetate → 4-(Dimethoxymethyl)pyrimidine

HRID 1897308
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인쇄 미리보기

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HRID 1897308 반응식
[CH3:1][N:2](C)/[CH:3]=[CH:4]/[C:5](=O)[CH:6]([O:9][CH3:10])[O:7][CH3:8].C(O)(=O)C.C(N)=[NH:18]>O>[CH3:8][O:7][CH:6]([O:9][CH3:10])[C:5]1[CH:4]=[CH:3][N:2]=[CH:1][N:18]=1
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참가 물질

4

반응물 2

HCID 160693Formamidine acetateHCID 5709580((1E)-4,4-dimethoxy-3-oxobut-1-en-1-yl)dimethylamine

생성물 1

HCID 124402404-(Dimethoxymethyl)pyrimidine수율 70.3%

시약·촉매·용매 1

HCID 962Water용매

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온도
120 °C

실험 절차

A mixture of (E)-4-dimethylamino-1,1-dimethoxy-but-3-en-2-one (49.6 g, 286 mmol) and formamidine acetate (44.7 g, 429 mmol) was heated at 120° C. for 4 h. After cooling to room temperature the mixture was poured into water and extracted with dichloromethane. The combined organic extracts were then dried over sodium sulfate, filtered and evaporated. Purification by distillation afforded the title product (31 g, 70%) as a colourless liquid. Bp 59-60° C. at 1.3 mbar. MS: m/e=155.0 [M+H]+.

후처리

  1. temperatureAfter cooling to room temperature the mixture
  2. extractionextracted with dichloromethane
  3. dry with materialThe combined organic extracts were then dried over sodium sulfate
  4. filtrationfiltered
  5. customevaporated
  6. customPurification
  7. distillationby distillation

출처 및 근거

ORD 기록
ord-0c8f84a1d3984636a18143a07ef77403
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08518974B2

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