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

Hydrochloric Acid → 4-Methylpentane-2,3-dione 2-oxime

HRID 1984962
노트
인쇄 미리보기

반응식

HRID 1984962 반응식
[CH3:1][CH:2]([C:4](=[O:7])[CH2:5][CH3:6])[CH3:3].Cl.[N:9](OCCC(C)C)=[O:10]>COC(C)(C)C.COCCOC>[CH3:1][CH:2]([CH3:3])[C:4](=[O:7])[C:5](=[N:9][OH:10])[CH3:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 8053Isoamyl NitriteHCID 112652-Methyl-3-pentanone

생성물 1

HCID 573574754-Methylpentane-2,3-dione 2-oxime

시약·촉매·용매 2

HCID 80711,2-Dimethoxyethane용매HCID 15413tert-Butyl methyl ether용매2회

실험 절차

100 g (948 mmol) of 2-methylpentan-3-one were dissolved in 400 ml of tert-butyl methyl ether. 50 g (274 mmol) of solution of hydrochloride in ethylene glycol dimethyl ether (20%) were added. Subsequently, a solution of 117 g (949 mmol) isoamyl nitrite in 150 ml of tert-butyl methyl ether was added dropwise within 60 minutes. The solvent was removed fully under reduced pressure. The residue was taken up in 300 ml of n-heptane and concentrated again under reduced pressure. After 200 ml of n-heptane had been added, extraction was effected with 522 ml of sodium hydroxide solution (2 molar). After phase separation, the aqueous phase was washed with n-heptane. The aqueous phase was acidified by adding conc. hydrochloric acid. The product was isolated by filtration with suction, washed with water and dried at elevated temperature under reduced pressure.

후처리

  1. customThe solvent was removed fully under reduced pressure
  2. concentrationconcentrated again under reduced pressure
  3. additionAfter 200 ml of n-heptane had been added
  4. extractionextraction
  5. customAfter phase separation
  6. washthe aqueous phase was washed with n-heptane
  7. additionby adding conc. hydrochloric acid
  8. customThe product was isolated by filtration with suction
  9. washwashed with water
  10. customdried at elevated temperature under reduced pressure

출처 및 근거

ORD 기록
ord-0779af3861ca42238d8739716743da4b
출처 데이터셋
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07544809B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트