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Thionyl Chloride → (3,5-Dimethylphenoxy)acetyl chloride

HRID 2182866
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HRID 2182866 반응식
[CH3:1][C:2]1[CH:3]=[C:4]([CH:10]=[C:11]([CH3:13])[CH:12]=1)[O:5][CH2:6][C:7](O)=[O:8].S(Cl)([Cl:16])=O>C1C=CC=CC=1>[CH3:1][C:2]1[CH:3]=[C:4]([CH:10]=[C:11]([CH3:13])[CH:12]=1)[O:5][CH2:6][C:7]([Cl:16])=[O:8]
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참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 794053,5-Xylyloxyacetic acid

생성물 1

HCID 12761006(3,5-Dimethylphenoxy)acetyl chloride

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

To a solution of 3,5-dimethylphenoxyacetic acid (9.0 g, 50 mmole) in benzene (100 mL) was added thionyl chloride (10.89 mL). The resulting mixture was refluxed for 2 hr, then the benzene was removed by distillation. The residual material was dried in vacuo to give 3,5-dimethylphenoxyacetyl chloride, which was dissolved in 20 ml of acetonitrile and used in situ. L-Glutamic acid (8.8 g, 60 mmole) was dissolved in a solution of sodium carbonate (12.72 g, 150 mL, 120 mmole) and the 3,5-dimethylphenoxyacetyl chloride in the acetonitrile solution was slowly added while the pH 8 was adjusted from time-to-time by adding sodium carbonate solution. The reaction mixture was stirred at room temperature for 2 hr, and acidified to pH 2 to give a solid precipitate. The solid precipitate was collected by filtration, treated with hot benzene, filtered, again and washed again with benzene to give Intermediate 31 (9.2 g).

후처리

  1. temperatureThe resulting mixture was refluxed for 2 hr
  2. customthe benzene was removed by distillation
  3. customThe residual material was dried in vacuo

출처 및 근거

ORD 기록
ord-a91d0d3067154b658caa749dd694328b
출처 데이터셋
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06897227B2

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