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

Hydrochloric Acid → p-Tolyl isobutyrate

HRID 1610713
노트
인쇄 미리보기

반응식

HRID 1610713 반응식
[Mg].II.[CH3:4][C:5]1[CH:12]=[CH:11][C:8]([CH2:9]Cl)=[CH:7][CH:6]=1.[C:13](#N)[CH:14]([CH3:16])[CH3:15].Cl.C([O:21]CC)C>>[CH3:15][CH:14]([CH3:16])[C:13](=[O:21])[CH2:9][C:8]1[CH:11]=[CH:12][C:5]([CH3:4])=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 6

HCID 313Hydrochloric AcidHCID 807IodineHCID 3283Diethyl Ether3회HCID 6559IsobutyronitrileHCID 77224-Methylbenzyl chlorideHCID 5462224Magnesium

생성물 1

HCID 13004936p-Tolyl isobutyrate

실험 절차

While stirring magnesium (22.5 g, 925 mmol) and iodine (1 crumb) in diethyl ether (400 ml), a solution of 4-methylbenzyl chloride (65.0 g, 463 mmol) in diethyl ether (500 ml) was dropwise added slowly at room temperature. After completion of the dropwise addition, the mixture was stirred at room temperature for 0.5 hr. To the reaction solution was added dropwise a solution of isobutyronitrile (21.31 g, 308.3 mmol) in diethyl ether (100 ml) under ice-cooling, and the mixture was stirred overnight at room temperature. To the reaction solution was added dropwise 1N hydrochloric acid under ice-cooling, and the mixture was stirred at room temperature for 1 hr. The diethyl ether layer was separated from the mixture, and the aqueous layer was extracted with diethyl ether. The recovered organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=15/1−9/1) to give the objective substance.

후처리

  1. additionAfter completion of the dropwise addition
  2. temperaturecooling
  3. stirringthe mixture was stirred overnight at room temperature
  4. temperaturecooling
  5. stirringthe mixture was stirred at room temperature for 1 hr
  6. customThe diethyl ether layer was separated from the mixture
  7. extractionthe aqueous layer was extracted with diethyl ether
  8. dry with materialThe recovered organic layer was dried over anhydrous magnesium sulfate
  9. customThe solvent was evaporated under reduced pressure
  10. customthe obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=15/1−9/1)
  11. customto give the objective substance

출처 및 근거

ORD 기록
ord-fc01ed19281b4a47a7761c9b5b4ef9ca
출처 데이터셋
uspto-grants-2006_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06982348B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트