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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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N-[4-(Hydroxymethyl)-1,3-thiazol-2-YL]acetamide → N-(4-Formyl-1,3-thiazol-2-YL)acetamide

HRID 1246421
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HRID 1246421 반응식
[OH:1][CH2:2][C:3]1[N:4]=[C:5]([NH:8][C:9](=[O:11])[CH3:10])[S:6][CH:7]=1>CO.C(Cl)(Cl)Cl.[O-2].[Mn+4].[O-2]>[CH:2]([C:3]1[N:4]=[C:5]([NH:8][C:9](=[O:11])[CH3:10])[S:6][CH:7]=1)=[O:1]
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참가 물질

5

반응물 1

HCID 14931748N-[4-(Hydroxymethyl)-1,3-thiazol-2-YL]acetamide

생성물 1

HCID 14931749N-(4-Formyl-1,3-thiazol-2-YL)acetamide수율 72.6%

시약·촉매·용매 3

HCID 178418406HCID 178418406, 화합물촉매HCID 887Methanol용매HCID 6212Chloroform용매

실험 절차

N-(4-(Hydroxymethyl)-1,3-thiazol-2-yl)acetamide (2.8 g) was dissolved in methanol (10 ml) and chloroform (200 ml). Then manganese (IV) oxide (28.3 g) was added to the solution under nitrogen atmosphere. The reaction mixture was stirred at room temperature for 7 hours, and filtered through a celite pad. The filtrate was concentrated in vacuo. The resulting solid was washed with ethyl ether to give N-(4-formyl-1,3-thiazol-2-yl)acetamide (2.01 g) as an off-white solid.

후처리

  1. filtrationfiltered through a celite pad
  2. concentrationThe filtrate was concentrated in vacuo
  3. washThe resulting solid was washed with ethyl ether

출처 및 근거

ORD 기록
ord-5b7ab3bdcaa848d9ba4b86a2f08a21d6
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07125901B2

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