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Hydrochloric Acid → 6-(4-Ethoxycarbonylbutyl)oxycoumarin

HRID 1533945
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HRID 1533945 반응식
[OH:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[O:8][C:7](=[O:12])[CH:6]=[CH:5]2.[H-].[Na+].Br[CH2:16][CH2:17][CH2:18][CH2:19][C:20]([O:22][CH2:23][CH3:24])=[O:21].Cl>CN(C)C=O>[CH2:23]([O:22][C:20]([CH2:19][CH2:18][CH2:17][CH2:16][O:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[O:8][C:7](=[O:12])[CH:6]=[CH:5]2)=[O:21])[CH3:24]
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참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 24758Sodium hydrideHCID 84580Ethyl 5-bromovalerateHCID 994776-hydroxy-2H-chromen-2-one

생성물 1

HCID 150296966-(4-Ethoxycarbonylbutyl)oxycoumarin

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
60 °C

실험 절차

6-Hydroxycoumarin (405 mg; prepared in reference example 25) was dissolved in dry dimethylformamide (6 ml). Sodium hydride (60 mg) was added to the solution. The mixture was reacted for 15 min. Ethyl 5-bromopentanoate (0.48 ml) was added dropwise to the reaction solution. The mixture was stirred for 1 hr at 60° C. Ice-water was added to the reaction solution. The mixture was acidified with 1N hydrochloric acid. The mixture was extracted with ether. The extract was washed with water, dried anhydrous magnesium sulfate and then evaporated. The residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate=4:1→2:1) to give the title compound (398 mg) having the following physical data.

후처리

  1. customThe mixture was reacted for 15 min
  2. extractionThe mixture was extracted with ether
  3. washThe extract was washed with water, dried anhydrous magnesium sulfate
  4. customevaporated
  5. customThe residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate=4:1→2:1)

출처 및 근거

ORD 기록
ord-f1a54e438bc84d6199a06072e4beaf57
출처 데이터셋
uspto-grants-1992_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05086065

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