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Sodium Cyanide → [5-Methyl-2-(4-trifluoromethyl-phenyl)-oxazol-4-yl]-acetonitrile

HRID 479131
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반응식

HRID 479131 반응식
[C-:1]#[N:2].[Na+].Cl[CH2:5][C:6]1[N:7]=[C:8]([C:12]2[CH:17]=[CH:16][C:15]([C:18]([F:21])([F:20])[F:19])=[CH:14][CH:13]=2)[O:9][C:10]=1[CH3:11]>CS(C)=O>[CH3:11][C:10]1[O:9][C:8]([C:12]2[CH:17]=[CH:16][C:15]([C:18]([F:21])([F:20])[F:19])=[CH:14][CH:13]=2)=[N:7][C:6]=1[CH2:5][C:1]#[N:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8929Sodium CyanideHCID 102363332-(4-Trifluoromethylphenyl)-4-chloromethyl-5-methyloxazole

생성물 1

HCID 18003422[5-Methyl-2-(4-trifluoromethyl-phenyl)-oxazol-4-yl]-acetonitrile

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매2회

실험 절차

To 5.39 g of NaCN (110 mol), dissolved in 72 ml of DMSO, was added via dropping funnel a solution of 19.57 g of the above prepared 4-chloromethyl-5-methyl-2-(4-trifluoromethyl-phenyl)-oxazole in 144 ml of DMSO (slightly exothermic). The reaction mixture was then kept for 1 h at 35° C. and 40° C. for 1 night. The reaction mixture was then poured onto crashed ice/AcOEt, the organic layer washed with water and brine, dried over magnesium sulfate, and evaporated to dryness. Flash chromatography (SiO2, hexane/AcOEt=8/2) delivered 8.81 g of the title compound as light yellow crystals of mp. 85-86°.

후처리

  1. additionwas added
  2. additionThe reaction mixture was then poured
  3. washthe organic layer washed with water and brine
  4. dry with materialdried over magnesium sulfate
  5. customevaporated to dryness

출처 및 근거

ORD 기록
ord-5510624caeca4c8c9df38b41fd26b79e
출처 데이터셋
uspto-grants-2003_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06642389B2

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