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Ethyl bromoacetate → ethyl (2,4-dioxo-2H-3,1-benzoxazin-1(4H)-yl)acetate

HRID 539856
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인쇄 미리보기

반응식

HRID 539856 반응식
[C:1]12[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=1)[NH:6][C:5](=[O:12])[O:4][C:2]2=[O:3].[H-].[Na+].Br[CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18]>CN(C)C=O>[O:12]=[C:5]1[N:6]([CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18])[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:1]=2[C:2](=[O:3])[O:4]1
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참가 물질

5

반응물 3

HCID 7748Ethyl bromoacetateHCID 8359Isatoic AnhydrideHCID 24758Sodium hydride

생성물 1

HCID 3568603ethyl (2,4-dioxo-2H-3,1-benzoxazin-1(4H)-yl)acetate

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

실험 절차

Isatoic anhydride (10 g, 1 equiv) in dimethylformamide (30 ml) was added dropwise to a suspension of sodium hydride (2.45 g, 60% in mineral oil, 1 equiv) in dimethylformamide (70 ml) at room temperature. The reaction was stirred for 1 hour prior to the addition of ethyl bromoacetate (6.8 ml, 1 equiv) and the resulting mixture stirred for 16 hours. Solvent evaporated, the residue suspended in water and the solid collected. The title compound was obtained by crystallisation from ethyl acetate (10.5 g). 1H-NMR (CDCl3) δ 1.29 (3H, t), 4.27 (2H, q), 4.82 (2H, s), 6.96 (1H, d), 7.33 (1H, t), 7.74 (1H, dt), 8.19 (1H, dd).

후처리

  1. stirringthe resulting mixture stirred for 16 hours
  2. customSolvent evaporated
  3. customthe solid collected

출처 및 근거

ORD 기록
ord-72bcf90349b34f89ba636c3cc8d37c11
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08871775B2

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