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Acetone → HCID 59655945, 화합물

HRID 2054451
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HRID 2054451 반응식
[CH3:1][C:2]([CH3:4])=O.S(=O)(=O)(O)O.[Br:10][C:11]1[CH:17]=[C:16]([CH3:18])[C:15]([CH3:19])=[CH:14][C:12]=1[NH2:13].[BH4-].[Na+]>O1CCCC1>[Br:10][C:11]1[CH:17]=[C:16]([CH3:18])[C:15]([CH3:19])=[CH:14][C:12]=1[NH:13][CH:2]([CH3:4])[CH3:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 180AcetoneHCID 1118Sulfuric AcidHCID 41792362-bromo-4,5-dimethylanilineHCID 4311764Sodium borohydride

생성물 1

HCID 59655945HCID 59655945, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of acetone (5.60 mL, 76.3 mmol) and aqueous 4 M sulfuric acid (5.20 mL, 20.8 mmol) in tetrahydrofuran (15 mL) was added dropwise to a stirred solution of 2-bromo-4,5-dimethylaniline 1-8 (13.9 g, 69.3 mmol) in tetrahydrofuran (40 mL) at approximately 0° C. Sodium borohydride (2.62 g, 69.3 mmol) was added cautiously and the resulting mixture allowed to warm to ambient temperature. After 30 min, the reaction was quenched by the careful sequential addition of water (25 mL) and sodium hydroxide pellets (until strongly alkaline). The reaction mixture was extracted with tert-butyl methyl ether (150 mL) and the organic phase was washed with brine, dried (sodium sulfate) and concentrated in vacuo to give a crude residue. Purification of the crude residue by flash chromatography over silica gel (gradient elution; 0%-20% ethyl acetate/hexanes as eluent) afforded 1-9 as a clear, pale orange oil.

후처리

  1. customthe reaction was quenched by the careful sequential addition of water (25 mL) and sodium hydroxide pellets (until strongly alkaline)
  2. extractionThe reaction mixture was extracted with tert-butyl methyl ether (150 mL)
  3. washthe organic phase was washed with brine
  4. dry with materialdried (sodium sulfate)
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-c17a7f77ff3242d6838155ea91ff6892
출처 데이터셋
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07329673B2

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