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

Water → 4-(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-Heptadecafluoroundecoxy)benzaldehyde

HRID 1828988
노트
인쇄 미리보기

반응식

HRID 1828988 반응식
[C:1](=[O:4])([O-])[O-].[K+].[K+].[OH:7][C:8]1[CH:15]=[CH:14][CH:13]=[CH:12][C:9]=1C=O.[F:16][C:17]([F:44])([CH2:40][CH2:41][CH2:42]I)[C:18]([F:39])([F:38])[C:19]([F:37])([F:36])[C:20]([F:35])([F:34])[C:21]([F:33])([F:32])[C:22]([F:31])([F:30])[C:23]([F:29])([F:28])[C:24]([F:27])([F:26])[F:25].O>CN(C=O)C.CCOCC>[F:16][C:17]([F:44])([CH2:40][CH2:41][CH2:42][O:7][C:8]1[CH:9]=[CH:12][C:13]([CH:1]=[O:4])=[CH:14][CH:15]=1)[C:18]([F:38])([F:39])[C:19]([F:36])([F:37])[C:20]([F:34])([F:35])[C:21]([F:32])([F:33])[C:22]([F:31])([F:30])[C:23]([F:29])([F:28])[C:24]([F:27])([F:26])[F:25]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 962WaterHCID 6998SalicylaldehydeHCID 11430Potassium CarbonateHCID 111575823-(Perfluorooctyl)propyl iodide

생성물 1

HCID 121541694-(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-Heptadecafluoroundecoxy)benzaldehyde수율 91%

시약·촉매·용매 2

HCID 3283
Diethyl Ether
용매
HCID 6228Dimethylformamide용매

반응 조건

온도
65 °C

실험 절차

A 500 mL 2-neck flask equipped with thermometer and gas inlet charged with potassium carbonate (27.6 g), hydroxy benzaldehyde (13.4 g), and 3-(perfluorooctyl)propyl iodide (58.8 g) in DMF (200 mL) was heated to 65° C. (internal temperature). The mixture was stirred at 65° C. until the reaction was complete. The reaction mixture was cooled to room temperature. Water (300 mL) and ether (300 mL) were added and the mixture stirred vigorously for 5 min. The layers were separated and the organic layer retained. The aqueous layer was extracted with ether (3×200 mL). The combined organic layers were washed with water (2×100 mL), Na2S2O3 (1×100 mL), 2.5 N NaOH (3×100 mL), and aqueous NaCl (1×100 mL). The organic layer was dried over MgSO4, filtered and concentrated. The product was further dried under high vacuum for 5 h to give desired product (53 g, 91% yield). The structure of the product was characterized 1H NMR.

후처리

  1. customA 500 mL 2-neck flask equipped with thermometer and gas inlet
  2. temperatureThe reaction mixture was cooled to room temperature
  3. stirringthe mixture stirred vigorously for 5 min
  4. customThe layers were separated
  5. extractionThe aqueous layer was extracted with ether (3×200 mL)
  6. washThe combined organic layers were washed with water (2×100 mL), Na2S2O3 (1×100 mL), 2.5 N NaOH (3×100 mL), and aqueous NaCl (1×100 mL)
  7. dry with materialThe organic layer was dried over MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe product was further dried under high vacuum for 5 h

출처 및 근거

ORD 기록
ord-200b91d81514479c960948f51b247c24
출처 데이터셋
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07060850B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트