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Dimethyl Sulfide → 6-nitro-3,4-dihydro-2H-1,4-benzoxazine

HRID 74062
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HRID 74062 반응식
S(C)C.[N+:4]([C:7]1[CH:8]=[CH:9][C:10]2[O:15][CH2:14][C:13](=O)[NH:12][C:11]=2[CH:17]=1)([O-:6])=[O:5]>C1COCC1>[N+:4]([C:7]1[CH:8]=[CH:9][C:10]2[O:15][CH2:14][CH2:13][NH:12][C:11]=2[CH:17]=1)([O-:6])=[O:5]
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참가 물질

4

반응물 2

HCID 1068Dimethyl SulfideHCID 27636836-Nitro-2H-1,4-benzoxazin-3(4H)-one

생성물 1

HCID 70622256-nitro-3,4-dihydro-2H-1,4-benzoxazine수율 89.5%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of BH3.Me2S in THF (2 M, 7.75 mL, 15.5 mmol) was added dropwise to a suspension of 6-nitro-4H-benzo[1,4]oxazin-3-one (0.6 g, 3.1 mmol) in THF (10 mL). The mixture was stirred at room temperature overnight. The reaction was quenched with MeOH (5 mL) at 0° C. and then water (20 mL) was added. The mixture was extracted with Et2O and the combined organic layers were washed with brine, dried over Na2SO4 and concentrated to give 6-nitro-3,4-dihydro-2H-benzo[1,4]oxazine as a red solid (0.5 g, 89%), which was used without further purification.

후처리

  1. customThe reaction was quenched with MeOH (5 mL) at 0° C.
  2. additionwater (20 mL) was added
  3. extractionThe mixture was extracted with Et2O
  4. washthe combined organic layers were washed with brine
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-c6aa03eb385c434599bcefdaaac81f0c
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08829204B2

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