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Hydrochloric Acid → HCID 12920232, 화합물

HRID 2261287
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HRID 2261287 반응식
[CH3:1][C:2]([CH3:16])([C:4](=O)[C:5]#[C:6][CH2:7][O:8]C1CCCCO1)[CH3:3].C[O-].[Na+].Cl.[NH2:21][OH:22].Cl.C(=O)([O-])O.[Na+]>CO>[C:2]([C:4]1[CH:5]=[C:6]([CH2:7][OH:8])[O:22][N:21]=1)([CH3:16])([CH3:3])[CH3:1]
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참가 물질

7

반응물 5

HCID 313Hydrochloric AcidHCID 443297Hydroxyamine hydrochlorideHCID 516892Sodium BicarbonateHCID 10942334Sodium MethoxideHCID 109552072,2-dimethyl-6-(tetrahydro-2H-pyran-2-yloxy)-4-hexyn-3-one

생성물 1

HCID 12920232HCID 12920232, 화합물수율 36.1%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
70 °C

실험 절차

4.49 g of 2,2-dimethyl-6-(tetrahydro-2H-pyran-2-yloxy)-4-hexyn-3-one was dissolved in 20 ml of methanol, and 1.30 g of sodium methoxide and 1.53 g of hydroxylamine hydrochloride were added. The mixture was stirred at 70° C. for 2 hours. The reaction mixture was cooled to room temperature and then adjusted to pH 2 with concentrated hydrochloric acid. The mixture was stirred at room temperature for 18 hours. After aqueous saturated sodium hydrogen carbonate was added, the reaction mixture was extracted with ethyl acetate. The extract was washed with aqueous saturated sodium chloride, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 1.12 g of (3-t-butyl-isoxazol-5-yl)methanol.

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. stirringThe mixture was stirred at room temperature for 18 hours
  3. extractionthe reaction mixture was extracted with ethyl acetate
  4. washThe extract was washed with aqueous saturated sodium chloride
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-c93a3c5a5b41463ea504659dc142aa7c
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07846956B2

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