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

Triethylamine → 9H-Fluoren-9-YL acrylate

HRID 2194325
노트
인쇄 미리보기

반응식

HRID 2194325 반응식
[OH:1][CH:2]1[C:14]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[C:8]2[C:3]1=[CH:4][CH:5]=[CH:6][CH:7]=2.C(N(CC)CC)C.[C:22](Cl)(=[O:25])[CH:23]=[CH2:24]>C1C=CC=CC=1>[CH:13]1[C:14]2[CH:2]([O:1][C:22](=[O:25])[CH:23]=[CH2:24])[C:3]3[C:8](=[CH:7][CH:6]=[CH:5][CH:4]=3)[C:9]=2[CH:10]=[CH:11][CH:12]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 13140Acryloyl chlorideHCID 74318Fluoren-9-ol

생성물 1

HCID 579315729H-Fluoren-9-YL acrylate수율 73%

시약·촉매·용매 1

HCID 241Benzene용매2회

반응 조건

온도
8 °C

실험 절차

To a 250 mL round-bottomed flask was added 9-hydroxyfluorene (5 g, 27.4 mmol) and triethylamine (3.86 ml, 27.4 mmol) in benzene (150 mL) to give a colorless solution. The solution was cooled to 8° C. with an ice bath. Next, acryloyl chloride (2.229 mL, 27.4 mmol) was dissolved in 25 mL of benzene, placed in a dropping funnel, and added over 1 hour with vigorous stirring. The reaction formed a white precipitate. The ice bath was removed and the viscous sludge was stirred overnight at room temperature. The resulting cloudy white suspension was washed with 50 mL water, followed by 50 mL 5% NaOH solution, and 50 mL water. The benzene layer was collected and dried with MgSO4, filtered, and rotovapped to give the 9-fluorenylacrylate as a viscous beige oil which crystallized on cooling to 4° C. (4.73 g, 20.02 mmol, 73.0% yield).

후처리

  1. customto give a colorless solution
  2. customplaced in a dropping funnel
  3. additionadded over 1 hour with vigorous stirring
  4. customThe reaction formed a white precipitate
  5. customThe ice bath was removed
  6. washThe resulting cloudy white suspension was washed with 50 mL water
  7. customThe benzene layer was collected
  8. dry with materialdried with MgSO4
  9. filtrationfiltered

출처 및 근거

ORD 기록
ord-31841909e770484fbd5e10ccd5d213ec
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08334026B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트