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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium Nitrite → HCID 178472910, 화합물

HRID 324424
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HRID 324424 반응식
[N:1]([O-:3])=O.[Na+].[CH3:5][C:6]1[CH:7]=[C:8]([CH2:12][CH2:13][C:14](=[O:21])[CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])[CH:9]=[CH:10][CH:11]=1>O.C(O)(=O)C>[OH:3][N:1]=[C:15]([C:14](=[O:21])[CH2:13][CH2:12][C:8]1[CH:9]=[CH:10][CH:11]=[C:6]([CH3:5])[CH:7]=1)[C:16]([O:18][CH2:19][CH3:20])=[O:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 23668193Sodium NitriteHCID 54309110Ethyl 3-oxo-5-m-toluylpentanoate

생성물 1

HCID 178472910HCID 178472910, 화합물

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 962Water용매2회

실험 절차

Sodium nitrite (32 g) in water (60 ml) was added dropwise over 1 hour to a stirred solution of the product from example 13 step (i) (99.4 g) in acetic acid (200 ml) at a rate such that the internal temperature did not rise above 30° C. The solution was allowed to stir a further 1 hour before adding water (500 ml). After stirring for a further 24 h the reaction mixture was extracted with diethyl ether (×4). The combined ether extracts were washed with saturated sodium bicarbonate solution, and finally water before collecting the organic layer and drying over magnesium sulphate. The solution was filtered and the solvent evaporated under reduced pressure to leave the subtitle product.

후처리

  1. customdid not rise above 30° C
  2. stirringAfter stirring for a further 24 h the reaction mixture
  3. extractionwas extracted with diethyl ether (×4)
  4. washThe combined ether extracts were washed with saturated sodium bicarbonate solution, and finally water
  5. custombefore collecting the organic layer
  6. dry with materialdrying over magnesium sulphate
  7. filtrationThe solution was filtered
  8. customthe solvent evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-9cf04f13af854fc48aded8d0d453957a
출처 데이터셋
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06218376B1

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