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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Oxalyl chloride → 4-Chloro-o-tolyloxyacetic acid chloride

HRID 639277
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HRID 639277 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

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 immediately began. After 30 minutes, the reaction mixture was warmed in a 45° 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 evaporated again in vacuo. Finally, dry toluene was added to the residue and this was evaporated at reduced pressure. The prepared acid chloride was used without further purification in the following step.

후처리

  1. customBubbling immediately
  2. temperaturethe reaction mixture was warmed in a 45° oil bath for 1.5 hours
  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 evaporated again in vacuo
  7. additionFinally, dry toluene was added to the residue
  8. customthis was evaporated at reduced pressure
  9. customThe prepared acid chloride was used without further purification in the following step

출처 및 근거

ORD 기록
ord-594526c534df4505af199cd70ad81f75
출처 데이터셋
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07691848B2

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