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Hydroxyamine hydrochloride → (E)-4-methyl-5-p-tolylpent-4-enenitrile

HRID 2408257
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HRID 2408257 반응식
[CH3:1]/[C:2](=[CH:7]\[C:8]1[CH:13]=[CH:12][C:11]([CH3:14])=[CH:10][CH:9]=1)/[CH2:3][CH2:4][CH:5]=O.Cl.[NH2:16]O>C(O)C>[CH3:1]/[C:2](=[CH:7]\[C:8]1[CH:13]=[CH:12][C:11]([CH3:14])=[CH:10][CH:9]=1)/[CH2:3][CH2:4][C:5]#[N:16]
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참가 물질

4

반응물 2

HCID 443297Hydroxyamine hydrochlorideHCID 714656444-Pentenal, 4-methyl-5-(4-methylphenyl)-, (4E)-

생성물 1

HCID 58390602(E)-4-methyl-5-p-tolylpent-4-enenitrile수율 70%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

(4E)-4-methyl-5-(4-methylphenyl)-4-pentenal (3.2 g, 0.017 mol) and hydroxylamine hydrochloride (1.77 g, 0.025 mol) were heated together in 95% ethyl alcohol (55 ml) at reflux for 4 hours. After cooling to room temperature, ethanol was removed on the rotavapor. The residue was stirred in diethyl ether (250 ml) for 30 minutes. The solid was filtered off, rinsed with diethyl ether and discarded. The filtrate was evaporated under vacuum. The product was purified by column chromatography on silica gel (eluent: heptane/ethyl acetate 11:1) followed by bulb-to-bulb distillation. 2.18 g of the desired compound were obtained (0.012 mol, 70% yield).

후처리

  1. temperatureat reflux for 4 hours
  2. customethanol was removed on the rotavapor
  3. filtrationThe solid was filtered off
  4. washrinsed with diethyl ether
  5. customThe filtrate was evaporated under vacuum
  6. customThe product was purified by column chromatography on silica gel (eluent: heptane/ethyl acetate 11:1)
  7. distillationfollowed by bulb-to-bulb distillation

출처 및 근거

ORD 기록
ord-d9ed61a99fb04ea088e6347f2f564dc0
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08815792B2

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