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2-Amino-4-(trifluoromethyl)phenol → 2-ChloroMethyl-5-trifluoroMethyl-benzooxazole

HRID 1772284
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HRID 1772284 반응식
[Cl:1][CH2:2][C:3]([O:10][CH2:11][CH3:12])(OCC)OCC.[NH2:13][C:14]1[CH:19]=[C:18]([C:20]([F:23])([F:22])[F:21])[CH:17]=CC=1O>C(O)(=O)C>[Cl:1][CH2:2][C:3]1[O:10][C:11]2[CH:12]=[CH:17][C:18]([C:20]([F:23])([F:22])[F:21])=[CH:19][C:14]=2[N:13]=1
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참가 물질

4

반응물 2

HCID 1202462-Amino-4-(trifluoromethyl)phenolHCID 3059222-Chloro-1,1,1-triethoxyethane

생성물 1

HCID 151337512-ChloroMethyl-5-trifluoroMethyl-benzooxazole수율 77%

시약·촉매·용매 1

HCID 176Acetic Acid용매

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온도
120 °C

실험 절차

2-Chloro-1,1,1-triethoxyethane (410 μL, 2.15 mmol) was added to a suspension of 2-amino-4-trifluoromethylphenol (370 mg, 1.79 mmol) in acetic acid (7 mL); during the addition the solution began to clear. The solution was heated at 120° C. (external temperature). After three hours the reaction mixture was cooled and the volatiles were removed under reduced pressure. Purification by silica gel chromatography, eluting with a gradient of 0 to 10% ethyl acetate in heptanes, gave 2-chloromethyl-5-trifluoromethyl-benzoxazole as a yellow oil (324 mg, 77%). (CI, m/z): [M+H]+ 236; 1H NMR (CDCl3): δ 8.05 (s, 1H), 7.66-7.73 (m, 2H), 4.79 (s, 2H); 19F NMR (376 MHz, CDCl3): δ ppm −61.26 (s, 3F).

후처리

  1. additionduring the addition the solution
  2. temperatureAfter three hours the reaction mixture was cooled
  3. customthe volatiles were removed under reduced pressure
  4. customPurification by silica gel chromatography
  5. washeluting with a gradient of 0 to 10% ethyl acetate in heptanes

출처 및 근거

ORD 기록
ord-461639f1df16415685603abe2b8a8c9c
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09249102B2

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