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Phosphorus oxychloride → 3-Chloro-5-chloro-2-methylquinoxaline

HRID 2044917
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HRID 2044917 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[C:9](O)[C:8]([CH3:13])=[N:7]2.P(Cl)(Cl)([Cl:16])=O>[NH4+].[OH-]>[Cl:16][C:9]1[C:8]([CH3:13])=[N:7][C:6]2[C:11]([N:10]=1)=[C:2]([Cl:1])[CH:3]=[CH:4][CH:5]=2
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참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 178432149HCID 178432149, 화합물

생성물 1

HCID 577078723-Chloro-5-chloro-2-methylquinoxaline

시약·촉매·용매 1

HCID 14923Ammonium Hydroxide용매

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온도
100 °C

실험 절차

A mixture of 8-chloro-3-methylquinoxalin-2-ol (1.0765 g, 5.5314 mmol) and phosphorous oxychloride (10.127 mL, 110.63 mmol) was stirred at 100° C. After 3 h, the mixture was cooled to room temperature. The mixture was poured into ice (˜100 mL) with stirring and neutralized with NH4OH (30 mL) and ice with stirring. The resulting precipitate was collected by filtration, rinsed with water (200 mL), and dried to give 3,5-dichloro-2-methylquinoxaline as a pink solid: 1H NMR (400 MHz, DMSO-d6) δ ppm 7.98-8.07 (2 H, m), 7.84 (1 H, dd, J=8.3, 7.7 Hz), 2.79 (3 H, s); LC-MS (ESI) m/z 213.0 [M+H]+. The pink solid was carried on crude without purification for the next step.

후처리

  1. temperaturethe mixture was cooled to room temperature
  2. stirringwith stirring
  3. stirringwith stirring
  4. filtrationThe resulting precipitate was collected by filtration
  5. washrinsed with water (200 mL)
  6. customdried

출처 및 근거

ORD 기록
ord-57656815253a4cca931967ab624dc7fd
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08586739B2

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