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Hydroxyamine hydrochloride → N-hydroxy-1-(4-methyl-1,2,5-thiadiazol-3-yl)-1-phenylmethanimine

HRID 2039684
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HRID 2039684 반응식
[CH3:1][C:2]1[C:3]([C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=O)=[N:4][S:5][N:6]=1.Cl.[NH2:16][OH:17]>N1C=CC=CC=1>[OH:17][N:16]=[C:7]([C:3]1[C:2]([CH3:1])=[N:6][S:5][N:4]=1)[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1
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참가 물질

4

반응물 2

HCID 443297Hydroxyamine hydrochlorideHCID 11830534(4-Methyl-1,2,5-thiadiazol-3-yl)(phenyl)methanone

생성물 1

HCID 136351090N-hydroxy-1-(4-methyl-1,2,5-thiadiazol-3-yl)-1-phenylmethanimine수율 99.6%

시약·촉매·용매 1

HCID 1049Pyridine용매

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온도
70 °C

실험 절차

To a stirred solution of (4-Methyl-[1,2,5]thiadiazol-3-yl)-phenyl-methanone (20 g, 98 mmol) in dry pyridine (70 mL) was added hydroxylamine hydrochloride (17 g, 245 mmol). The reaction mixture was stirred at 70° C. for 3 h, then concentrated in vacuo and diluted with ethyl acetate (100 mL) and water (100 mL). The organic layer was washed with water (2×100 mL) and dried over MgSO4. Evaporation of the solvent in vacuo afforded N-hydroxy-1-(4-methyl-1,2,5-thiadiazol-3-yl)-1-phenylmethanimine as an orange oil [24.3 g, yield 99.6%; HPLC/MS: m/z=220 (M+H); log P(HCOOH)=2.26].

후처리

  1. concentrationconcentrated in vacuo
  2. additiondiluted with ethyl acetate (100 mL) and water (100 mL)
  3. washThe organic layer was washed with water (2×100 mL)
  4. dry with materialdried over MgSO4
  5. customEvaporation of the solvent in vacuo

출처 및 근거

ORD 기록
ord-b3177ab24c444568863fd73d9c0d5201
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08580799B2

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