Methyl fluorosulfate → 4-Cyano-3,5-dichloro-2-methylisothiazolium fluorosulfonate

反応式

[C:1]([C:3]1[C:4]([Cl:9])=[N:5][S:6][C:7]=1[Cl:8])#[N:2].[F:10][S:11]([O:14][CH3:15])(=[O:13])=[O:12]>>[F:10][S:11]([O-:14])(=[O:13])=[O:12].[C:1]([C:3]1[C:4]([Cl:9])=[N+:5]([CH3:15])[S:6][C:7]=1[Cl:8])#[N:2]

参加物

反応物 2

HCID 9870Methyl fluorosulfate

HCID 305706Dichloro-1,2-thiazole-4-carbonitrile

生成物 1

HCID 128890284-Cyano-3,5-dichloro-2-methylisothiazolium fluorosulfonate収率 92%

実験手順

4-Cyano-3,5-dichloroisothiazole (5.0 g, 0.028 mol) and 4 ml of methyl fluorosulfonate were heated at 80°-90° for 30 min under a nitrogen atmosphere. The resulting solid was washed with ether and benzene to yield 7.5 g (92%) of 4-cyano-3,5-dichloro-2-methylisothiazolium fluorosulfonate, mp 160-170. Spectral data (NMR and IR) were consistent with the assigned structure. Analysis-calculated for C5H3Cl2FN2O3S2 : C, 20.50; H, 1.02; Found: C, 20.27; H, 1.44.

後処理

washThe resulting solid was washed with ether and benzene

出典と根拠

ORDレコード: ord-6b03cf8ca22e47268f60e3e04a8e500b
出典データセット: uspto-grants-1985_04
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US04508908

反応ノート

読み込み中…

参加物