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

Dimethylformamide → 4-Methoxybenzamide

HRID 2240203
노트
인쇄 미리보기

반응식

HRID 2240203 반응식
C([C:8]1[CH:16]=[C:15]([O:17][CH3:18])[CH:14]=[CH:13][C:9]=1[C:10](O)=[O:11])C1C=CC=CC=1.C[N:20](C=O)C.C(Cl)(=O)C(Cl)=O>C(Cl)Cl>[CH3:18][O:17][C:15]1[CH:14]=[CH:13][C:9]([C:10]([NH2:20])=[O:11])=[CH:8][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 65578Oxalyl chlorideHCID 225559782-Benzyl-4-methoxybenzoic acid

생성물 1

HCID 769594-Methoxybenzamide

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To a solution of 2-benzyl-4-methoxybenzoic acid (14.2 g) in 600 mL CH2Cl2 was added a catalytic amount of DMF, followed by a solution of oxalyl chloride (8.7 g) in 100 mL of CH2Cl2. The reaction was stirred at room temp overnight, then concentrated and azeotroped with toluene (2×). The residue was dissolved in 700 mL CH2Cl2 and cooled to 0 C. Tert-butyl amine (13.9 g) was added, and the reaction was warmed to room temp. After 1.5 h, the reaction was quenched with 5% aqueous KHSO4. The organic solution was separated, washed once with saturated aqueous sodium bicarbonate, dried (Na2SO4) and concentrated to give 15.9 g of 2-benzyl-N-tert-butyl)-4-methoxybenzamide.

후처리

  1. concentrationconcentrated
  2. customazeotroped with toluene (2×)
  3. dissolutionThe residue was dissolved in 700 mL CH2Cl2
  4. temperaturecooled to 0 C
  5. additionTert-butyl amine (13.9 g) was added
  6. temperaturethe reaction was warmed to room temp
  7. waitAfter 1.5 h
  8. customthe reaction was quenched with 5% aqueous KHSO4
  9. customThe organic solution was separated
  10. washwashed once with saturated aqueous sodium bicarbonate
  11. dry with materialdried (Na2SO4)
  12. concentrationconcentrated

출처 및 근거

ORD 기록
ord-7b726dcc643e41839b95d12f44fe52b9
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07723352B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트