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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Diethyl Ether → 99028-44-1

HRID 1788868
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HRID 1788868 반응식
Cl.[C:2](=[NH:7])([O:4][CH2:5][CH3:6])[CH3:3].C(N(CC)CC)C.[C:15](Cl)(=[O:17])[CH3:16].CCOCC>C(Cl)Cl>[C:15]([N:7]=[C:2]([O:4][CH2:5][CH3:6])[CH3:3])(=[O:17])[CH3:16]
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참가 물질

6

반응물 4

HCID 3283Diethyl EtherHCID 6367Acetyl chlorideHCID 8471TriethylamineHCID 2724290Ethanimidic acid, ethyl ester, hydrochloride (1:1)

생성물 1

HCID 1001191999028-44-1

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A slurry of 50.0 gm (405 mmol) of ethyl acetimidate hydrochloride in 500 ml of methylene chloride was mechanically stirred and treated dropwise with 81.9 gm (809 mmol) of triethylamine while keeping the temperature at less than 25° C. The resulting slurry was then treated dropwise with 31.8 gm (405 mmol) of acetyl chloride while keeping the temperature at less than 30° C. The white slurry was stirred for one hour at room temperature, after which the methylene chloride was removed in vacuo. The white, oily mass obtained was then stirred with 400 ml of ether and filtered. The white solid obtained was washed with additional ether and the combined filtrate was concentrated in vacuo to afford 48.6 gm (93 percent) of a pale, yellow oil. IR and NMR spectra were consistent with the assigned structure.

후처리

  1. customat less than 25° C
  2. customat less than 30° C
  3. customafter which the methylene chloride was removed in vacuo
  4. customThe white, oily mass obtained
  5. filtrationfiltered
  6. customThe white solid obtained
  7. washwas washed with additional ether
  8. concentrationthe combined filtrate was concentrated in vacuo
  9. customto afford 48.6 gm (93 percent) of a pale, yellow oil

출처 및 근거

ORD 기록
ord-a3f93e06bdb3443090fa16797409ab1b
출처 데이터셋
uspto-grants-1987_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04685958

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