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Oxalyl chloride → 4-Chloro-o-tolyloxyacetic acid chloride

HRID 2244292
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HRID 2244292 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[C:4]([O:9][CH2:10][C:11]([OH:13])=O)[CH:3]=1.C(Cl)(=O)C([Cl:17])=O>ClCCl.CN(C)C=O>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[C:4]([O:9][CH2:10][C:11]([Cl:17])=[O:13])[CH:3]=1
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참가 물질

5

반응물 2

HCID 65578Oxalyl chlorideHCID 164957292-(5-Chloro-2-methylphenoxy)acetic acid

생성물 1

HCID 1298977964-Chloro-o-tolyloxyacetic acid chloride

시약·촉매·용매 2

HCID 6228Dimethylformamide촉매HCID 6344Dichloromethane용매

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온도
45 °C

실험 절차

To a cold suspension of 4-chloro-o-tolyloxyacetic acid (17.4 mmol) in 40 mL of dry dichloromethane was added oxalyl chloride (39.15 mmol) followed by one drop of N,N-dimethylformamide. Bubbling began immediately. After 30 minutes the reaction mixture was warmed in a 45° C. oil bath for 1.5 hours. The solution was cooled to room temperature and all volatiles were removed by evaporation. Dry nitrogen gas was introduced into the evaporator and more dry dichloromethane was added. This was again evaporated in vacuo. Finally, dry toluene was added to the residue and this was evaporated at reduced pressure. The crude acid chloride was used without further purification in the following step.

후처리

  1. customBubbling
  2. temperatureThe solution was cooled to room temperature
  3. customall volatiles were removed by evaporation
  4. additionDry nitrogen gas was introduced into the evaporator and more dry dichloromethane
  5. additionwas added
  6. customThis was again evaporated in vacuo
  7. additionFinally, dry toluene was added to the residue
  8. customthis was evaporated at reduced pressure
  9. customThe crude acid chloride was used without further purification in the following step

출처 및 근거

ORD 기록
ord-9285cac1acaa4d6eaa2c3d5db4a543d2
출처 데이터셋
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07678787B2

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