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Hydroxylamine → N'-Hydroxy-N-(1-methylethyl)-N-phenylurea

HRID 1582564
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HRID 1582564 반응식
[NH2:1][OH:2].[CH3:3][CH:4]([N:6]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[C:7](Cl)=[O:8])[CH3:5]>C1COCC1>[OH:2][NH:1][C:7](=[O:8])[N:6]([CH:4]([CH3:5])[CH3:3])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1
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참가 물질

4

반응물 2

HCID 787HydroxylamineHCID 11446927(1-Methylethyl)phenylcarbamic chloride

생성물 1

HCID 22717691N'-Hydroxy-N-(1-methylethyl)-N-phenylurea수율 100%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A solution, of 50% aqueous hydroxylamine (16.8 g, 0.25 mol) was added dropwise to a solution of (1-methylethyl)phenylcarbamic chloride (20.0 g, 0.1 mol) in 200 mL of THF in an ice bath so that the reaction temperature was kept below 30° C. Precipitate began to form halfway through the addition. The resulting slurry was stirred overnight. The mixture was filtered, and the solids collected were first washed with water and then with hexane/ether. After air-drying, 14.56 g of the title compound was obtained. Its structure was confirmed by an analysis of the NMR spectra. The filtrate was stripped down to afford a residue which was washed sequentially with 1N HCl, water and hexane/ether to yield a second crop of the title compound (5.38 g) melting at 165-166° C. The combined yield was 100%.

후처리

  1. customwas kept below 30° C
  2. customto form halfway
  3. additionthrough the addition
  4. filtrationThe mixture was filtered
  5. customthe solids collected
  6. washwere first washed with water
  7. customAfter air-drying

출처 및 근거

ORD 기록
ord-349a02fa5caf422aba950ebbacbbbb0c
출처 데이터셋
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06737383B1

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