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Hydrochloric Acid → 2-(2,4-Dichloro-3-methylphenoxy)propanoic acid

HRID 358188
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HRID 358188 반응식
[Cl:1][C:2]1[C:15]([CH3:16])=[C:14]([Cl:17])[CH:13]=[CH:12][C:3]=1[O:4][CH:5]([CH3:11])[C:6]([O:8]CC)=[O:7].Cl>C(O)(=O)C>[Cl:1][C:2]1[C:15]([CH3:16])=[C:14]([Cl:17])[CH:13]=[CH:12][C:3]=1[O:4][CH:5]([CH3:11])[C:6]([OH:8])=[O:7]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 14721691HCID 14721691, 화합물

생성물 1

HCID 133669662-(2,4-Dichloro-3-methylphenoxy)propanoic acid수율 86.7%

시약·촉매·용매 1

HCID 176Acetic Acid용매

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온도
100 °C

실험 절차

In 100 ml of ethanol was dissolved 10.0 g. (0.05 mole) of sodium 2,4-dichloro-3-methylphenolate. With stirring at room temperature, 9.1 g (0.05 mole) of ethyl 2-bromopropionate was added. The mixture was heated under relfux for 4 hours. The ethanol was distilled off under reduced pressure, and the residue was extracted with 50 ml of diethyl ether. The ethereal layer was washed with 25 ml of a 5% aqueous solution of sodium hydroxide and 25 ml of water, and dried over anyhdrous magnesium sulfate. The dessicant was removed by filtration, and the diethyl ether was distilled off to give 11.8 g of crude ethyl 2-(2,4-dichloro-3-methylphenoxy)propionate. The crude ester (11.8 g) was dissolved in 100 ml of glacial acetic acid. Concentrated hydrochloric acid (25 ml) was added, and the mixture was stirred at 100° C. for 40 minutes. The reaction mixture was cooled, and poured onto 300 ml of ice water. The precipitated crystals were filtered, washed with water, and dried to give 9.2 g of 2-(2,4-dichloro-3-methylphenoxy)-propionic acid. The yield was 73.9% based on the sodium 2,4-dichloro-3-methylphenolate, and the final product had a melting point of 149.5 to 150.5° C.

후처리

  1. temperatureThe reaction mixture was cooled
  2. filtrationThe precipitated crystals were filtered
  3. washwashed with water
  4. customdried

출처 및 근거

ORD 기록
ord-c8a5be79d34945e998870050ca314750
출처 데이터셋
uspto-grants-1984_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04465507

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