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Dimethylformamide → 2-Chloro-5-nitrobenzo[d]oxazole

HRID 512450
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HRID 512450 반응식
S[C:2]1[O:3][C:4]2[CH:10]=[CH:9][C:8]([N+:11]([O-:13])=[O:12])=[CH:7][C:5]=2[N:6]=1.CN(C=O)C.S(Cl)([Cl:21])=O>>[Cl:21][C:2]1[O:3][C:4]2[CH:10]=[CH:9][C:8]([N+:11]([O-:13])=[O:12])=[CH:7][C:5]=2[N:6]=1
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참가 물질

4

반응물 3

HCID 6228DimethylformamideHCID 24386Thionyl ChlorideHCID 178526504HCID 178526504, 화합물

생성물 1

HCID 103527232-Chloro-5-nitrobenzo[d]oxazole

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온도
65 °C

실험 절차

Subsequently, the crude 2-mercapto-5-nitrobenzoxazole (10 g, 51 mmol), previously prepared, was dissolved in thionyl chloride (100 mL). DMF (60 μL) was added and the reaction mixture was heated at 65° C. for 45 min. After cooling, the solvent was removed under reduced pressure and to the residue, toluene was added twice (2×20 mL) and each time subsequently evaporated in vacuo to remove volatiles via azeotrope. The resultant crude product was dissolved in ethyl acetate (400 mL), washed with brine (200 mL), dried over Na2SO4, filtered, and concentrated to give compound 29, 2-chloro-5-nitrobenzoxazole, as (8.2 g, crude).

후처리

  1. temperatureAfter cooling
  2. customthe solvent was removed under reduced pressure and to the residue, toluene
  3. additionwas added twice (2×20 mL)
  4. customeach time subsequently evaporated in vacuo
  5. customto remove volatiles via azeotrope
  6. dissolutionThe resultant crude product was dissolved in ethyl acetate (400 mL)
  7. washwashed with brine (200 mL)
  8. dry with materialdried over Na2SO4
  9. filtrationfiltered
  10. concentrationconcentrated

출처 및 근거

ORD 기록
ord-a8933e70a14844059ac74a47cc63921b
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09102636B2

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