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

Triphenylphosphine → 3-(3,5-Difluorophenoxy)tetrahydro-2H-pyran

HRID 1499611
노트
인쇄 미리보기

반응식

HRID 1499611 반응식
[F:1][C:2]1[CH:3]=[C:4]([OH:9])[CH:5]=[C:6]([F:8])[CH:7]=1.[O:10]1[CH2:15][CH2:14][CH2:13][CH:12](O)[CH2:11]1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CC(OC(/N=N/C(OC(C)C)=O)=O)C>C1COCC1>[F:1][C:2]1[CH:3]=[C:4]([CH:5]=[C:6]([F:8])[CH:7]=1)[O:9][CH:12]1[CH2:13][CH2:14][CH2:15][O:10][CH2:11]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 11776TriphenylphosphineHCID 759283,5-DifluorophenolHCID 5363146Diisopropyl azodicarboxylateHCID 12256033tetrahydro-2H-pyran-3-ol

생성물 1

HCID 867268303-(3,5-Difluorophenoxy)tetrahydro-2H-pyran수율 75.8%

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매

실험 절차

A solution of 3,5-difluorophenol (1.15 g, 8.81 mmol), tetrahydro-2H-pyran-3-ol (0.900 g, 8.81 mmol), triphenylphosphine (2.31 g, 8.81 mmol) and DIAD (1.74 mL, 8.81 mmol) in THF (10 mL) was stirred overnight. The solution was then concentrated under reduced pressure and the residue was purified by purified by column chromatography on silica gel using CombiFlash® apparatus eluting with EtOAc/hexanes (0-30%). The purification afforded 1.43 g (75.8%) of the sub-title compound as a colorless oil.

후처리

  1. concentrationThe solution was then concentrated under reduced pressure
  2. customthe residue was purified
  3. customby purified by column chromatography on silica gel using CombiFlash® apparatus
  4. washeluting with EtOAc/hexanes (0-30%)
  5. customThe purification

출처 및 근거

ORD 기록
ord-b73e56504dc64af9833bbf63bd5b1540
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09200004B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트