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

4-Chlorobenzoic Acid → 4-Chloro-2-methylbenzoic acid

HRID 1018295
노트
인쇄 미리보기

반응식

HRID 1018295 반응식
[CH3:1]N(C)C(CC)CN(C)C.N#N.CCO.[Li]C(CC)C.[Cl:21][C:22]1[CH:30]=[CH:29][C:25]([C:26]([OH:28])=[O:27])=[CH:24][CH:23]=1.CI>C1COCC1>[Cl:21][C:22]1[CH:30]=[CH:29][C:25]([C:26]([OH:28])=[O:27])=[C:24]([CH3:1])[CH:23]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 63184-Chlorobenzoic AcidHCID 6328Methyl iodideHCID 12405076N,N,N',N'-tetramethylethylethylenediamineHCID 86585260Nitrogen ethanolHCID 178418400CID 53628100

생성물 1

HCID 3482694-Chloro-2-methylbenzoic acid수율 78.2%

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매

반응 조건

온도
-50 °C

실험 절차

In a dry round-bottomed flask (3 L) equipped with a mechanical stirrer under N2, anhydrous N,N,N′,N′-tetramethylethylethylenediamine (TMEDA, 99.7 mL, 660 mmol, 2.2 eq.) and anhydrous THF (600 mL) were added and the mixture was cooled to −90° C. in a bath of liquid N2/EtOH. Freshly titrated sec-BuLi (550 mL, 1.2M in cyclohexane, 660 mmol., 2.2 eq.) was added slowly via cannula as to maintain the temperature at −50° C. The solution was cooled to −90° C. and 4-chlorobenzoic acid (47.0 g in 400 mL anhydrous THF, 300 mmol) was added slowly via cannula, while stirring carefully to maintain the temperature at −90° C. The reaction mixture was stirred at −90° C. for 1 h before allowed to warm-up to −80° C. and CH3I (80 mL, 1.28 moles) was added very slowly. The reaction mixture was stirred for 10 min at −80° C., then quenched slowly with H2O (600 mL) and allowed to warm-up to room temperature. The aqueous layer was separated, washed with Et2O (2×500 mL) and then acidified with HCl (2.5 N, 600 mL) while cooling in an ice bath; cooling was continued for 16 h at 4° C. to allow crystallization of the desired product. The crude product was dried under vacuum and over anhydrous P2O5 and then re-crystallized from hot toluene (700 mL) to obtain pure 4-chloro-2-methylbenzoic acid (40 g).

후처리

  1. customIn a dry round-bottomed flask (3 L) equipped with a mechanical stirrer under N2
  2. temperatureThe solution was cooled to −90° C.
  3. temperatureto maintain the temperature at −90° C
  4. stirringThe reaction mixture was stirred at −90° C. for 1 h
  5. temperatureto warm-up to −80° C.
  6. stirringThe reaction mixture was stirred for 10 min at −80° C.
  7. customquenched slowly with H2O (600 mL)
  8. temperatureto warm-up to room temperature
  9. customThe aqueous layer was separated
  10. washwashed with Et2O (2×500 mL)
  11. temperaturewhile cooling in an ice bath
  12. temperaturecooling
  13. customcrystallization of the desired product
  14. dry with materialThe crude product was dried under vacuum and over anhydrous P2O5
  15. customre-crystallized from hot toluene (700 mL)

출처 및 근거

ORD 기록
ord-fc7d136a32fc4b559726038f0e47f33d
출처 데이터셋
uspto-grants-2002_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06479508B1

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트