反応式
[CH3:1][N:2]([C:16](F)=[O:17])[S:3][N:4]=[C:5]([S:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[CH:6]([CH3:8])[CH3:7].[CH3:19][C:20]1([CH3:30])[CH2:24][C:23]2[CH:25]=[CH:26][CH:27]=[C:28]([OH:29])[C:22]=2[O:21]1.C(OC(=O)C)C>[Cl-].C([N+](CC1C=CC=CC=1)(C)C)CCCCCCCCCCCCCCC.C(Cl)Cl.[OH-].[Na+].CCCCCC>[CH3:1][N:2]([C:16]([O:29][C:28]1[C:22]2[O:21][C:20]([CH3:30])([CH3:19])[CH2:24][C:23]=2[CH:25]=[CH:26][CH:27]=1)=[O:17])[S:3][N:4]=[C:5]([S:9][C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1)[CH:6]([CH3:8])[CH3:7]参加物
反応物 3
生成物 1
試薬・触媒・溶媒 4
実験手順
To a solution of phenyl N-[[methyl[fluorocarbonyl]amino]thio]-2-methylpropiothioimidate (7.8 g, 27 mmoles) as prepared in Preparation 1 and cetylbenzyldimethylammonium chloride (0.9 g) in methylene chloride (150 ml) is added a solution of 2,3-dihydro-2,2-dimethyl-7-benzofuranol (4.5 g, 27 mmoles) in 0.18N sodium hydroxide (150 ml). The two-phase reaction mixture is stirred vigorously at ambient temperature for 90 minutes. The layers are separated and the organic phase dried over anhydrous sodium sulfate. Removal of the solvent gives a clear brown oil. This material is transferred to a column of silica gel and the chromatogram developed with a solvent mixture consisting of 8% ethylacetate in Skellysolve B. From the appropriate fraction there is obtained a white solid which is recrystallized from hexane to give the product phenyl N-[[methyl[[[2,3-dihydro-2,2-dimethyl-7- benzofuranyl]oxy]carbonyl]amino]thio]-2-methyl-propiothioimidate as a white crystalline solid, mp 104°-106°.
後処理
- customThe two-phase reaction mixture
- customThe layers are separated
- dry with materialthe organic phase dried over anhydrous sodium sulfate
- customRemoval of the solvent
- customgives a clear brown oil
- customFrom the appropriate fraction there is obtained a white solid which
- customis recrystallized from hexane
出典と根拠
- ORDレコード
- ord-51ebf8ac035546169d8a39f23468747f
- 出典データセット
- uspto-grants-1986_06
- 特許番号
- US04592871
関連ノート
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