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Hydrochloric Acid → 2-(4-Chloro-2-ethynylphenyl)propanenitrile

HRID 1868849
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HRID 1868849 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH3:11])[C:9]#[N:10])=[C:4]([C:12]#[C:13][Si](C)(C)C)[CH:3]=1.[OH-].[Na+].Cl>C1COCC1>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH3:11])[C:9]#[N:10])=[C:4]([C:12]#[CH:13])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 670996472-(4-Chloro-2-(2-(trimethylsilyl)ethynyl)phenyl)propanenitrile

생성물 1

HCID 866292602-(4-Chloro-2-ethynylphenyl)propanenitrile

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 2-(4-chloro-2-(2-(trimethylsilyl)ethynyl)phenyl)-propanenitrile (0.550 g, 2.1 mmol) in THF (25 mL) was added 5N NaOH (15 mL). After one hour, the reaction was complete as determined by LC-MS and TLC. The solution was acidified with 5N HCl until the pH was about 2. The solution was extracted with EtOAc (3×40 mL). The combined organic layers were washed with water (2×30 mL) and brine (2×30 mL), dried with MgSO4, and concentrated in vacuo. The resulting orange oil was purified using silica flash chromatography on the ISCO with 0-20% EtOAc/hexanes. MS m/e=190 (M+H)+.

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후처리

  1. extractionThe solution was extracted with EtOAc (3×40 mL)
  2. washThe combined organic layers were washed with water (2×30 mL) and brine (2×30 mL)
  3. dry with materialdried with MgSO4
  4. concentrationconcentrated in vacuo
  5. customThe resulting orange oil was purified

출처 및 근거

ORD 기록
ord-89504feae8b3418c9fc9bf51ec05efc1
출처 데이터셋
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07635715B2

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