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Hydrochloric Acid → 6-Chloro-3-methyl-5-nitro-1,2-benzisothiazole

HRID 369600
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인쇄 미리보기

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HRID 369600 반응식
N(OC(C)(C)C)=O.N[C:9]1[C:18]([N+:19]([O-:21])=[O:20])=[CH:17][C:12]2[C:13]([CH3:16])=[N:14][S:15][C:11]=2[CH:10]=1.[ClH:22]>C(#N)C.[Cu](Cl)Cl>[Cl:22][C:9]1[C:18]([N+:19]([O-:21])=[O:20])=[CH:17][C:12]2[C:13]([CH3:16])=[N:14][S:15][C:11]=2[CH:10]=1
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참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 10906Tert-Butyl nitriteHCID 183144986-Amino-3-methyl-5-nitro-1,2-benzisothiazole

생성물 1

HCID 183144816-Chloro-3-methyl-5-nitro-1,2-benzisothiazole

시약·촉매·용매 2

HCID 24014Cupric Chloride촉매HCID 6342Acetonitrile용매

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온도
65 °C

실험 절차

A mixture of tert-butyl nitrite (3.30 mL, 0.0278 mol) and copper(II) chloride (2.98 g, 0.0222 mol) in acetonitrile is heated to 65° C., treated portionwise with 6-amino-3-methyl-5-nitro-1,2-benzisothiazole (3.88 g, 0.0185 mol), stirred at 65° C., cooled to room temperature, and poured into 20% hydrochloric acid. The resultant aqueous mixture is extracted with ethyl acetate. The organic extracts are combined, washed with 20% hydrochloric acid, dried over anhydrous magnesium sulfate, and concentrated in vacuo to obtain a solid. Flash column chromatography of the solid using silica gel and methylene chloride/hexanes solutions (1:1 and 3:1) gives the title product as a pale, yellow solid (2.54 g, mp 156-158° C.) which is identified by NMR spectral analyses.

후처리

  1. temperaturecooled to room temperature
  2. extractionThe resultant aqueous mixture is extracted with ethyl acetate
  3. washwashed with 20% hydrochloric acid
  4. dry with materialdried over anhydrous magnesium sulfate
  5. concentrationconcentrated in vacuo
  6. customto obtain a solid

출처 및 근거

ORD 기록
ord-e4c9bfcca00f4b17bfe02bab17789729
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06140270

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