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Hydrogen Peroxide → HCID 178440937, 화합물

HRID 1057760
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HRID 1057760 반응식
[OH:1]O.[CH2:3]([C:7]1[CH:14]=[CH:13][C:10]([C:11]#[N:12])=[C:9]([OH:15])[N:8]=1)[CH2:4][CH:5]=[CH2:6]>CCO.[OH-].[Na+]>[CH2:3]([C:7]1[CH:14]=[CH:13][C:10]([C:11]([NH2:12])=[O:1])=[C:9]([OH:15])[N:8]=1)[CH2:4][CH:5]=[CH2:6]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 784Hydrogen PeroxideHCID 178440933HCID 178440933, 화합물

생성물 1

HCID 178440937HCID 178440937, 화합물수율 100%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 14798Sodium Hydroxide용매

반응 조건

온도
50 °C

실험 절차

Hydrogen peroxide (30 wt. % solution in water, 45 mL) was added to a solution of a1 (12.13 g, 70.2 mmol) in a mixture of EtOH (150 mL) and 10% aqueous NaOH (280 mL) at 23° C. The reaction mixture was heated to 50° C. for 18 h, then was cooled to 23° C. and the volatiles were removed under reduced pressure. The residue was acidified with 12 M HCl to pH 2-3, and the resulting precipitate was filtered, washed with water (2×50 mL), and air-dried to afford b1 as a yellow solid (13.48 g, 100%): mp=195-198° C.; IR (cm−1) 3329, 3134, 1688, 1642; 1H NMR (DMSO-d6) δ 2.31-2.38 (m, 2H), 2.64 (t, 2H, J=7.6), 4.96-5.05 (m, 2H), 5.71-5.84 (m, 1H), 6.29 (d, 1H, J=7.3), 7.45 (s, br, 1H), 8.21 (d, 1H, J=7.3), 9.00 (s, br, 1H), 12.37 (s, br, 1H); Anal. C10H12N2O2·0.15H2O: C, H, N.

후처리

  1. temperaturewas cooled to 23° C.
  2. customthe volatiles were removed under reduced pressure
  3. filtrationthe resulting precipitate was filtered
  4. washwashed with water (2×50 mL)
  5. customair-dried

출처 및 근거

ORD 기록
ord-88de84d4eefc4b03bc5fd8fcb66d97c3
출처 데이터셋
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06514997B2

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