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Ethyl bromoacetate → HCID 86657404, 화합물

HRID 400551
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HRID 400551 반응식
[C:1](=[C:4]([C:7]#[N:8])[C:5]#[N:6])([CH3:3])[CH3:2].Br[CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12]>[Zn].C1COCC1>[C:5]([CH:4]([C:7]#[N:8])[C:1]([CH3:3])([CH3:2])[CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12])#[N:6]
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참가 물질

5

반응물 2

HCID 7748Ethyl bromoacetateHCID 533473Isopropylidenemalononitrile

생성물 1

HCID 86657404HCID 86657404, 화합물

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 8028Tetrahydrofuran용매

실험 절차

Zinc powder (1.23 g, 18.85 mmol) was added to a THF (20 mL) solution of isopropylidenemalononitrile (1.0 g, 9.42 mmol), ethyl bromoacetate (3.15 g, 18.85 mmol) and titanium bis(cyclopentadienyl)dichloride (235 mg, 0.94 mmol). After stirring for 1 hour the solution was partitioned between ethyl acetate and aqueous 1N HCl. The organic phase was washed with water, brine, dried over MgSO4 and filtered. The solution was concentrated and the crude residue purified by silica gel chromatography using a hexanes/EtOAc gradient to give the indicated product. 1H NMR (400 MHz, CD3CN): δ 4.55 (s, 1H); 4.10 (q, J=7.2 Hz, 2H); 2.48 (s, 2H); 1.24 (s, 6H); 1.21 (t, J=7.2 Hz, 3H).

후처리

  1. customwas partitioned between ethyl acetate and aqueous 1N HCl
  2. washThe organic phase was washed with water, brine
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. concentrationThe solution was concentrated
  6. customthe crude residue purified by silica gel chromatography
  7. customto give the indicated product

출처 및 근거

ORD 기록
ord-056a7d17be4143729c1f902598e7527c
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08741910B2

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