Lithium cyanide → HCID 19982141, 화합물
반응식
[F:1][C:2]1[CH:3]=[CH:4][C:5]2[S:10][CH2:9][CH:8]([CH2:11][C:12](O)=O)[CH2:7][C:6]=2[CH:15]=1.F[C:17]1[CH:18]=[CH:19][C:20]2SCC(CI)CC=2[CH:28]=1.[C-]#[N:30].[Li+]>CN(C)C=O>[F:1][C:2]1[CH:3]=[CH:4][C:5]2[S:10][CH2:9][CH:8]([CH2:11][CH2:12][N:30]3[CH2:20][CH2:19][CH2:18][CH2:17][CH2:28]3)[CH2:7][C:6]=2[CH:15]=1참가 물질
실험 절차
The starting material is prepared as follows: 6-Fluoro-3,4-dihydro-2H-1-benzothiopyran-3-ylacetic acid: A mixture of 3.8 g 6-fluoro-3-iodomethyl-3,4-dihydro-2H-1-benzothiopyran and 30 ml 0.5 M lithium cyanide in dimethylformamide is stirred at room temperature for 24 hours after which it is poured onto water. The product is extracted with ether. After drying over magnesium sulfate the solvent is removed in vacuo. This residue is refluxed in a mixture of 20 ml acetic acid and 20 ml 12 N HCl for 6 hours. The solvent is removed in vacuo, the residue is dissolved in 1 N NaOH and washed with ether. The aqueous phase is acidified with 3 N HCl and the product is extracted with ether. After drying over magnesium sulfate, the solvent is removed in vacuo. The residue is triturated with ether/hexane and affords the title compound, m.p. 125°-135° C.
후처리
- customThe starting material is prepared
- additionis poured onto water
- extractionThe product is extracted with ether
- dry with materialAfter drying over magnesium sulfate the solvent
- customis removed in vacuo
- temperatureThis residue is refluxed in a mixture of 20 ml acetic acid and 20 ml 12 N HCl for 6 hours
- customThe solvent is removed in vacuo
- dissolutionthe residue is dissolved in 1 N NaOH
- washwashed with ether
- extractionthe product is extracted with ether
- dry with materialAfter drying over magnesium sulfate
- customthe solvent is removed in vacuo
- customThe residue is triturated with ether/hexane
출처 및 근거
- ORD 기록
- ord-40c2335ba801451facf2944ada010a17
- 출처 데이터셋
- uspto-grants-1991_12
- 특허 번호
- US05071858
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