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Acetic Anhydride → HCID 4547045, 화합물

HRID 2233341
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HRID 2233341 반응식
[CH2:1]([C:4]1[CH:11]=[CH:10][CH:9]=[C:6]([CH:7]=O)[C:5]=1[OH:12])[CH:2]=[CH2:3].CCN(CC)CC.[C:20](OC(=O)C)(=[O:22])[CH3:21]>C(OCC)(=O)C>[CH2:1]([C:4]1[CH:11]=[CH:10][CH:9]=[C:6]2[C:5]=1[O:12][C:20](=[O:22])[CH:21]=[CH:7]2)[CH:2]=[CH2:3]
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참가 물질

5

반응물 3

HCID 7918Acetic AnhydrideHCID 8471TriethylamineHCID 1410623-Allylsalicylaldehyde

생성물 1

HCID 4547045HCID 4547045, 화합물수율 40%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

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온도
160 °C

실험 절차

To a solution of 3-allylsalicylaldehyde (1.62 g, 10.0 mmol) in acetic anhydride (2 mL) in a 5 mL Emrys process vial was added Et3N (2.0 ml). The reaction was heated at 160° C. for 45 min in an Emrys Optimizer Microwave reactor then was cooled to RT. The reaction was diluted with 50 mL of ethyl acetate, the organic layer was washed with aqueous ammonium chloride, aqueous sodium chloride, dried (Na2SO4), and concentrated. Purification of the residue by flash chromatography on silica gel (gradient elution: 5% to 30% Ethyl acetate/Hexanes) yielded the title compound (750 mg, 40%) as a colorless oil: MS (ES) m/e 186.9 (M+H)+.

후처리

  1. temperaturethen was cooled to RT
  2. washthe organic layer was washed with aqueous ammonium chloride, aqueous sodium chloride
  3. dry with materialdried (Na2SO4)
  4. concentrationconcentrated
  5. customPurification of the residue by flash chromatography on silica gel (gradient elution: 5% to 30% Ethyl acetate/Hexanes)

출처 및 근거

ORD 기록
ord-20b931ed34534304aa1e71ffba2dd053
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07709496B2

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