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

Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester → HCID 131734416, 화합물

HRID 587863
노트
인쇄 미리보기

반응식

HRID 587863 반응식
[C:1]12([O:16][CH2:15][CH2:14][O:13]1)[C:10]1[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=1)[CH2:4][C@@H:3]([CH:11]=O)[CH2:2]2.C1(P(C2C=CC=CC=2)(C2C=CC=CC=2)=[CH:24][C:25]([O:27][CH2:28][CH3:29])=[O:26])C=CC=CC=1>C(Cl)Cl>[C:1]12([O:16][CH2:15][CH2:14][O:13]1)[C:10]1[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=1)[CH2:4][C@@H:3]([CH:11]=[CH:24][C:25]([O:27][CH2:28][CH3:29])=[O:26])[CH2:2]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 70670Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl esterHCID 118324708HCID 118324708, 화합물

생성물 1

HCID 131734416HCID 131734416, 화합물수율 46.2%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To the stirred solution of (R)-3′,4′-dihydro-2′H-spiro[[1,3]dioxolane-2,1′-naphthalene]-3′-carbaldehyde (4.1 g, 18.79 mmol) in DCM (10 mL), ethyl 2-(triphenyl phosphoranylidene)acetate (7.85 g, 22.54 mmol) was added and reaction mixture was stirred at RT for 16 h. After completion of reaction, reaction mixture was concentrated under vacuum to get 5.5 g of crude compound. This crude compound was further purified by flash chromatography (Biotage) using eluent hexane/ethyl acetate 80:20 to get the title compound (2.5 g, 46.2% yield); m/z 288.34

후처리

  1. customreaction mixture
  2. customAfter completion of reaction, reaction mixture
  3. concentrationwas concentrated under vacuum
  4. customto get 5.5 g of crude compound
  5. customThis crude compound was further purified by flash chromatography (Biotage)

출처 및 근거

ORD 기록
ord-e45f515da89d48d2bab69870791f80aa
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09227919B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트