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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Diethyl Ether → HCID 71743245, 화합물

HRID 1423067
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HRID 1423067 반응식
[Br:1][C:2]1[CH:7]=[C:6]([CH2:8][C:9]#[N:10])[CH:5]=[CH:4][N:3]=1.Br[CH2:12][CH2:13]Br.CCOCC.[H-].[Na+]>CS(C)=O.CCOC(C)=O.O>[Br:1][C:2]1[CH:7]=[C:6]([C:8]2([C:9]#[N:10])[CH2:13][CH2:12]2)[CH:5]=[CH:4][N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 3283Diethyl EtherHCID 78391,2-DibromoethaneHCID 24758Sodium hydrideHCID 534290262-(2-Bromopyridin-4-YL)acetonitrile

생성물 1

HCID 71743245HCID 71743245, 화합물

시약·촉매·용매 3

HCID 679Dimethyl Sulfoxide용매2회
HCID 962
Water
용매
HCID 8857Ethyl Acetate용매

실험 절차

A solution of (2-bromopyridin-4-yl)-acetonitrile (1.20 g, 6.09 mmol) and the 1,2-dibromoethane (0.663 mL, 7.61 mmol) in a mixture of anhydrous Et2O (5 mL) and anhydrous DMSO (1 mL) is added to a suspension of NaH (60% dispersion in mineral oil, 585 mg, 14.6 mmol) in anhydrous DMSO (10 mL) while controlling the resulting exotherm by cooling in a water bath, and the resulting mixture is stirred at room temperature. After 18 hours, water (10 mL) and EtOAc (10 mL) are added, phases are separated and the aqueous layer is extracted with EtOAc (3×10 mL). The combined organic layers are washed with brine (30 mL) and dried over MgSO4, filtered and concentrated. The residue is purified by silica gel chromatography eluting with a gradient of 0-60% EtOAc in heptane to afford 1-(2-bromopyridin-4-yl)-cyclopropanecarbonitrile as a solid. MS m/z 223.4, 225.4.

후처리

  1. temperatureby cooling in a water bath
  2. customphases are separated
  3. extractionthe aqueous layer is extracted with EtOAc (3×10 mL)
  4. washThe combined organic layers are washed with brine (30 mL)
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue is purified by silica gel chromatography
  9. washeluting with a gradient of 0-60% EtOAc in heptane

출처 및 근거

ORD 기록
ord-20a1c9eb12dd4aa78a9a2c52053a0dd3
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08927550B2

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