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Hydrochloric Acid → 2-Chloro-4,6-difluorobenzothiazole

HRID 9567
ノート
印刷プレビュー

反応式

HRID 9567 の反応式
N(OCCC(C)C)=O.[F:9][C:10]1[C:15]2[N:16]=[C:17](N)[S:18][C:14]=2[CH:13]=[C:12]([F:20])[CH:11]=1.[ClH:21]>C(#N)C.[Cu](Cl)Cl>[Cl:21][C:17]1[S:18][C:14]2[CH:13]=[C:12]([F:20])[CH:11]=[C:10]([F:9])[C:15]=2[N:16]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 313Hydrochloric AcidHCID 8053Isoamyl NitriteHCID 7374064,6-Difluoro-1,3-benzothiazol-2-amine

生成物 1

HCID 20498832-Chloro-4,6-difluorobenzothiazole収率 99%

試薬・触媒・溶媒 2

HCID 24014Cupric Chloride触媒HCID 6342Acetonitrile溶媒

実験手順

To a solution containing copper chloride (II) (0.87 g, 6.45 mmol) and tri(ethylene glycol) dimethyl ether (3 mL) in acetonitrile (50 mL) was added isoamyl nitrite (0.94 g, 8.06 mmol), and the reaction mixture was stirred at rt for 30 minutes. To this suspension was added dropwise a solution of 4,6-difluoro-1,3-benzothiazol-2-amine (1.0 g, 5.37 mmol) in tri(ethylene glycol) dimethyl ether (5 mL). The reaction mixture was stirred at rt for 10 minutes, and then heated at 50° C. for 2.5 h. The reaction mixture was cooled to rt, and then poured cautiously into cold aqueous 6 M HCl (200 mL). The solution was extracted with EtOAc. The organic layer was washed with HCl (1.0 M), water and brine, filtered and concentrated down to afford 2-chloro-4,6-difluoro-1,3-benzothiazole (1.1 g, 99%). 1H NMR (400 MHz, DMSO-d6) 7.05 (m, 1H), 7.36 (m, 1H).

後処理

  1. stirringThe reaction mixture was stirred at rt for 10 minutes
  2. temperatureheated at 50° C. for 2.5 h
  3. temperatureThe reaction mixture was cooled to rt
  4. extractionThe solution was extracted with EtOAc
  5. washThe organic layer was washed with HCl (1.0 M), water and brine
  6. filtrationfiltered
  7. concentrationconcentrated down

出典と根拠

ORDレコード
ord-b1d3138809e7413ab40947cf032e2724
出典データセット
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07091228B2

反応ノート

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