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Water → (2,2-Dichloro-3,3-dimethylcyclopropyl)acetonitrile

HRID 1981334
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HRID 1981334 반응식
C1(C)C=CC(S(O[CH2:11][CH:12]2[C:14]([CH3:16])([CH3:15])[C:13]2([Cl:18])[Cl:17])(=O)=O)=CC=1.[C-:20]#[N:21].[K+].O>CN(C)C=O>[Cl:18][C:13]1([Cl:17])[C:14]([CH3:15])([CH3:16])[CH:12]1[CH2:11][C:20]#[N:21]
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참가 물질

5

반응물 3

HCID 962WaterHCID 9032Potassium CyanideHCID 13313521HCID 13313521, 화합물

생성물 1

HCID 13313532(2,2-Dichloro-3,3-dimethylcyclopropyl)acetonitrile수율 106.5%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
100 °C

실험 절차

6.48 g of 2,2-dichloro-3,3-dimethylcyclopropylmethyl p-toluenesulfonate and 2.0 g of potassium cyanide were suspended in 20 ml of dimethyl formamide, and the mixture was heated at 100° C. for 24 hours with stirring. After cooling, 50 ml of water was added to the reaction mixture. The mixture was extracted with hexane. The hexane layer was washed with water, and dried over sodium sulfate. After drying, the hexane was evaporated under reduced pressure to give 3.8 g of 2,2-dichloro-3,3-dimethylcyclopropylacetonitrile, the desired compound shown above. The boiling point of the product was 96° to 98° C. at 14 mmHg.

후처리

  1. temperatureAfter cooling
  2. extractionThe mixture was extracted with hexane
  3. washThe hexane layer was washed with water
  4. dry with materialdried over sodium sulfate
  5. customAfter drying
  6. customthe hexane was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-be4af018903341bd8ac5651fc55f3388
출처 데이터셋
uspto-grants-1985_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04514418

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