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

Pyridine → 1,1-Dimethylethyl 4-methylbenzoate

HRID 965542
노트
인쇄 미리보기

반응식

HRID 965542 반응식
[C:1]([OH:5])([CH3:4])([CH3:3])[CH3:2].N1C=CC=CC=1.[C:12]1([CH3:21])[CH:17]=[CH:16][C:15]([C:18](Cl)=[O:19])=[CH:14][CH:13]=1>O>[CH3:21][C:12]1[CH:17]=[CH:16][C:15]([C:18]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:19])=[CH:14][CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1049PyridineHCID 6386tert-ButanolHCID 134054-Methylbenzoyl Chloride

생성물 1

HCID 116297491,1-Dimethylethyl 4-methylbenzoate수율 80.1%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

37 g of tert-butanol and then 26 ml of pyridine are added to 39.04 g of p-toluoyl chloride and the reaction mixture is refluxed for 3 hours. After cooling, it is poured into water, extracted with AcOEt, washed with a 1N solution of HCl and then with a 5% solution of sodium hydrogencarbonate, dried over sodium sulfate and evaporated under vacuum. The residue is chromatographed on silica using hexane and then a hexane/DCM mixture (80/20; v/v) as the eluent to give 38.9 g of the expected product, which is used as such in the next step.

후처리

  1. temperaturethe reaction mixture is refluxed for 3 hours
  2. temperatureAfter cooling
  3. extractionextracted with AcOEt
  4. washwashed with a 1N solution of HCl
  5. dry with materialwith a 5% solution of sodium hydrogencarbonate, dried over sodium sulfate
  6. customevaporated under vacuum
  7. customThe residue is chromatographed on silica

출처 및 근거

ORD 기록
ord-464e26a0daa5479c900cd57dd7066397
출처 데이터셋
uspto-grants-1998_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05773612

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트