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

Pentanal → 1-(3,5-Difluorophenyl)pentan-1-ol

HRID 327370
노트
인쇄 미리보기

반응식

HRID 327370 반응식
[CH:1](=[O:6])[CH2:2][CH2:3][CH2:4][CH3:5].Br[C:8]1[CH:13]=[C:12]([F:14])[CH:11]=[C:10]([F:15])[CH:9]=1.[Mg].[Cl-].[NH4+]>CCOCC.C1COCC1>[F:14][C:12]1[CH:13]=[C:8]([CH:1]([OH:6])[CH2:2][CH2:3][CH2:4][CH3:5])[CH:9]=[C:10]([F:15])[CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 8063PentanalHCID 25517Ammonium ChlorideHCID 1363131-Bromo-3,5-difluorobenzeneHCID 5462224Magnesium

생성물 1

HCID 225984431-(3,5-Difluorophenyl)pentan-1-ol수율 116%

시약·촉매·용매 2

HCID 3283Diethyl Ether용매
HCID 8028
Tetrahydrofuran
용매

실험 절차

A solution of pentanal (19.0 g, 0.22 mol) in dry ether (75 ml) is added dropwise to a stirred solution of the Grignard reagent at room temperature, under dry nitrogen, prepared from 1-bromo-3,5-difluoro-benzene (50.2 g, 0.26 mol) and magnesium (7.25 g, 0.30 mol) in dry THF (100 ml). The stirred mixture is heated under reflux for 2 h, cooled and a saturated solution of ammonium chloride (300 ml) is added. The product is extracted into ether (twice), and the combined ethereal extracts are washed with water and dried (MgSO4). The solvent is removed in vacuo to give a pale-orange liquid (51.1 g) which is distilled to yield a colourless liquid. Smaller quantities of crude product are purified by column chromatography (silica gel/dichloromethane) to yield a colourless liquid, bp 90° C. at 0.5 mm Hg.

후처리

  1. temperatureThe stirred mixture is heated
  2. temperatureunder reflux for 2 h
  3. temperaturecooled
  4. extractionThe product is extracted into ether (twice), and the combined ethereal extracts
  5. washare washed with water
  6. dry with materialdried (MgSO4)
  7. customThe solvent is removed in vacuo

출처 및 근거

ORD 기록
ord-076640e60e0f4a54abc6f912cc20b302
출처 데이터셋
uspto-grants-1993_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05273680

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트