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Trimethylsilyl cyanide → HCID 13672817, 화합물

HRID 1732014
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HRID 1732014 반응식
[CH:1]1[C:10]2[C:9]3[CH:11]=[CH:12][CH:13]=[CH:14][C:8]=3[CH:7](O)[S:6][C:5]=2[CH:4]=[CH:3][CH:2]=1.C[Si]([C:20]#[N:21])(C)C>C1C=CC=CC=1.[Zn+2].[I-].[I-]>[C:20]([CH:7]1[S:6][C:5]2[CH:4]=[CH:3][CH:2]=[CH:1][C:10]=2[C:9]2[CH:11]=[CH:12][CH:13]=[CH:14][C:8]1=2)#[N:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 82115Trimethylsilyl cyanideHCID 13153992HCID 13153992, 화합물

생성물 1

HCID 13672817HCID 13672817, 화합물

시약·촉매·용매 2

HCID 9883512zinc(II)iodide촉매HCID 241Benzene용매

실험 절차

6H-dibenzo[b,d]thiopyran-6-ol (2.6 g; 12 mmol) was dissolved in anhydrous benzene (50 ml). Trimethylsilylcyanide (4.5 ml; 36 mmol) and a catalytic amount of ZnI2 were added to the solution, then the reaction mixture was stirred for 20 hours at room temperature. The solution was washed with 1N NaOH, dried and evaporated. The residue was crystallized from diethyl ether to give 6-cyano-6H-dibenzo[b,d]thiopyran as white solid (2.3 g; 10 mmol); m.p. 114°-116° C. By proceeding analogously the following compounds were obtained:

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후처리

  1. washThe solution was washed with 1N NaOH
  2. customdried
  3. customevaporated
  4. customThe residue was crystallized from diethyl ether

출처 및 근거

ORD 기록
ord-0dc182d6cfdb4b4f89c631919520c558
출처 데이터셋
uspto-grants-1986_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04624949

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