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Nitroethane → 2-Hydroxy-4-methoxybenzonitrile

HRID 719120
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HRID 719120 반응식
[OH:1][C:2]1[CH:9]=[C:8]([O:10][CH3:11])[CH:7]=[CH:6][C:3]=1[CH:4]=O.C([O-])(=O)C.[Na+].[N+:17](CC)([O-])=O>C(O)(=O)C>[OH:1][C:2]1[CH:9]=[C:8]([O:10][CH3:11])[CH:7]=[CH:6][C:3]=1[C:4]#[N:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6587NitroethaneHCID 696002-Hydroxy-4-MethoxybenzaldehydeHCID 517045Sodium Acetate

생성물 1

HCID 114236802-Hydroxy-4-methoxybenzonitrile수율 86%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

A mixture of the 2-hydroxy-4-methoxybenzaldehyde (20 g, 128.8 mmol), sodium acetate (35.05 g, 257.6 mmol) and nitroethane (19 mL, 257.6 mmol) in glacial acetic acid (100 mL) was heated at gentle reflux for 12 h. The reaction mixture was then poured into ˜1000 mL of ice water (1:1 ratio of ice and water). The product was extracted with ethyl acetate (3×200 mL). The organic extracts were washed with sodium bicarbonate solution until the aqueous layer had pH ˜8. The organic layers were then dried over anhydrous magnesium sulfate and concentrated in vacuo to afford 2-hydroxy-4-methoxy-benzonitrile as a yellow oil (16.5 g, 86%). It was used without further purification.

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후처리

  1. temperaturewas heated
  2. temperatureat gentle reflux for 12 h
  3. extractionThe product was extracted with ethyl acetate (3×200 mL)
  4. washThe organic extracts were washed with sodium bicarbonate solution until the aqueous layer
  5. dry with materialThe organic layers were then dried over anhydrous magnesium sulfate
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-e5a769c3bc2d4c87bb9b20d92c92ebdd
출처 데이터셋
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07132421B2

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