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Dichloromethane → 3,5-Dinitrobenzaldehyde

HRID 1280184
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HRID 1280184 반응식
C(Cl)(=O)C(Cl)=O.C(Cl)Cl.[N+:10]([C:13]1[CH:14]=[C:15]([CH:18]=[C:19]([N+:21]([O-:23])=[O:22])[CH:20]=1)[CH2:16][OH:17])([O-:12])=[O:11].C(N(CC)CC)C>C1COCC1.O>[N+:10]([C:13]1[CH:14]=[C:15]([CH:18]=[C:19]([N+:21]([O-:23])=[O:22])[CH:20]=1)[CH:16]=[O:17])([O-:12])=[O:11]
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7

반응물 4

HCID 6344DichloromethaneHCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 1169783,5-Dinitrobenzyl alcohol

생성물 1

HCID 17123033,5-Dinitrobenzaldehyde수율 89%

시약·촉매·용매 2

HCID 962Water용매
HCID 8028
Tetrahydrofuran
용매

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온도
-65 °C

실험 절차

To a solution of oxalylchloride (26 ml, 0.30 mol) in CH2Cl2 (600 ml) DMSO (43 ml, 0.60 mol) was added, maintaining the temperature between −50° C. and −65° C. To the reaction solution was then added 3,5-dinitrobenzyl alcohol (50g), in THF (100 ml), maintaining the temperature between −50° C. and −65° C. The reaction mixture was stirred at −65° C. for 30 minutes and then triethylamine (170 ml) was added at −50° C. and −65° C. The reaction temperature was then adjusted to room temperature and H2O (800 ml) was added. The organic phase was washed with sat. NaHCO3 (500 ml), 5 times with diluted HCl (300 ml) and finally brine. The organic phase was then dried over MgSO4 and the volatile solvents were removed at reduced pressure. The crude product was then triturated with heptane, which gave 45.8 g (89%) of 3,5-dinitrobenzaldehyde.

후처리

  1. temperaturemaintaining the temperature between −50° C. and −65° C
  2. customwas then adjusted to room temperature
  3. washThe organic phase was washed with sat. NaHCO3 (500 ml), 5 times with diluted HCl (300 ml) and finally brine
  4. dry with materialThe organic phase was then dried over MgSO4
  5. customthe volatile solvents were removed at reduced pressure
  6. customThe crude product was then triturated with heptane, which

출처 및 근거

ORD 기록
ord-559a51bd6d514a9ea7d285f4b0c5ae81
출처 데이터셋
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06448442B1

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