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(Diethylamino)sulfur trifluoride → 2-(3-(alpha-Fluorobenzyl)phenyl)-[1,3]-dioxolane

HRID 1666783
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인쇄 미리보기

반응식

HRID 1666783 반응식
[O:1]1[CH2:5][CH2:4][O:3][CH:2]1[C:6]1[CH:7]=[C:8]([CH:12]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)O)[CH:9]=[CH:10][CH:11]=1.C(N(S(F)(F)[F:26])CC)C>ClCCl>[F:26][CH:12]([C:8]1[CH:7]=[C:6]([CH:2]2[O:3][CH2:4][CH2:5][O:1]2)[CH:11]=[CH:10][CH:9]=1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 123472(Diethylamino)sulfur trifluorideHCID 10824966(3-[1,3]Dioxolan-2-ylphenyl)phenylmethanol

생성물 1

HCID 210714122-(3-(alpha-Fluorobenzyl)phenyl)-[1,3]-dioxolane

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
-78 °C

실험 절차

Combine (3-[1,3]-dioxolan-2-ylphenyl)phenylmethanol (2.3 g, 8.9 mmol) and dichloromethane (50 ml). Cool to about −78° C. Add dropwise a solution of (diethylamino)sulfur trifluoride (1.7 ml, 12.9 mmol). After 10 minutes, quench with water and extract with dichloromethane. Combine the organic layers and wash sequentially with distilled water and brine and then dry (Na2SO4), filter, and concentrate to give a residue. Chromatograph the residue eluting with 7:3 hexane:EtOAc to give the title compound.

후처리

  1. customquench with water
  2. extractionextract with dichloromethane
  3. washwash sequentially with distilled water and brine
  4. dry with materialdry (Na2SO4)
  5. filtrationfilter
  6. concentrationconcentrate
  7. customto give a residue
  8. washChromatograph the residue eluting with 7:3 hexane

출처 및 근거

ORD 기록
ord-7ce8b06cc6c04105a234c4d3671baf02
출처 데이터셋
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08044090B2

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