홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Sodium Bicarbonate → 4-Methyl-5-propionyloxazole

HRID 2797
노트
인쇄 미리보기

반응식

HRID 2797 반응식
CON(C)[C:4]([C:6]1[O:10][CH:9]=[N:8][C:7]=1[CH3:11])=[O:5].[CH2:13]([Mg]Br)[CH3:14].C(=O)([O-])O.[Na+]>O1CCCC1>[CH3:11][C:7]1[N:8]=[CH:9][O:10][C:6]=1[C:4](=[O:5])[CH2:13][CH3:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 516892Sodium BicarbonateHCID 18925369N-Methoxy-N,4-dimethyloxazole-5-carboxamideHCID 178418443HCID 178418443, 화합물

생성물 1

HCID 189363294-Methyl-5-propionyloxazole

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

N-Methoxy-N-methyl-4-methyl-5-oxazolecarboxamide (5 g) in dry tetrahydrofuran at -40° C. was stirred under a nitrogen atmosphere and ethylmagnesium bromide (1M solution in tetrahydrofuran, 35 ml) was added dropwise. After 30 minutes the mixture was allowed to warm to room temperature and then stirred for a further 1 hour. Aqueous sodium hydrogen carbonate was added, the organic layer was separated and the aqueous layer was extracted with diethylether. The material thus obtained was purified by flash chromatography to yield a pale yellow liquid which solidified on cooling.

후처리

  1. customthe organic layer was separated
  2. extractionthe aqueous layer was extracted with diethylether
  3. customThe material thus obtained
  4. customwas purified by flash chromatography
  5. customto yield a pale yellow liquid which
  6. temperatureon cooling

출처 및 근거

ORD 기록
ord-1bc1f72b809c473ca26027a1470cdec4
출처 데이터셋
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05731335

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트