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Hydrochloric Acid → Ethyl 5-(3-chlorophenyl)-3-oxopentanoate

HRID 324441
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인쇄 미리보기

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HRID 324441 반응식
[Li+].CC([N-]C(C)C)C.[C:9]([O:15][CH2:16][CH3:17])(=[O:14])[CH2:10][C:11]([CH3:13])=[O:12].[Cl:18][C:19]1[CH:20]=[C:21]([CH:24]=[CH:25][CH:26]=1)[CH2:22]Br.Cl>O1CCCC1>[Cl:18][C:19]1[CH:20]=[C:21]([CH2:22][CH2:13][C:11](=[O:12])[CH2:10][C:9]([O:15][CH2:16][CH3:17])=[O:14])[CH:24]=[CH:25][CH:26]=1
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참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 8868Ethyl AcetoacetateHCID 698381-(Bromomethyl)-3-chlorobenzeneHCID 2724682Lithium diisopropylamide

생성물 1

HCID 20462750Ethyl 5-(3-chlorophenyl)-3-oxopentanoate

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
0 °C

실험 절차

To a solution of LDA (2.0M solution in heptanes/tetrahydrofuran/ethylbenzene, 500 ml) in tetrahydrofuran (2 L) at 0° C. was added ethyl acetoacetate (62 ml). After 40 min 3-chlorobenzyl bromide (100 g) was added dropwise and the mixture was stirred at 0° C. for 1 hour. The reaction mixture was acidified with 2N HCl and the organic phase was concentrated under reduced pressure. The residue was dissolved in ethyl acetate and washed with water and brine, dried (MgSO4) and evaporated. Purification was by chromatography eluting with 5-10% ethyl acetate in isohexane.

후처리

  1. concentrationthe organic phase was concentrated under reduced pressure
  2. dissolutionThe residue was dissolved in ethyl acetate
  3. washwashed with water and brine
  4. dry with materialdried (MgSO4)
  5. customevaporated
  6. customPurification
  7. washeluting with 5-10% ethyl acetate in isohexane

출처 및 근거

ORD 기록
ord-597121b0d5e947ce86f54bee3d04c4c6
출처 데이터셋
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06218376B1

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