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Ethyl bromoacetate → [7-Methyl-6-(methyloxy)-3-oxo-2,3-dihydro-4H-1,4-benzoxazin-4-yl]acetic acid

HRID 2354354
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HRID 2354354 반응식
[CH3:1][C:2]1[C:12]([O:13][CH3:14])=[CH:11][C:5]2[NH:6][C:7](=[O:10])[CH2:8][O:9][C:4]=2[CH:3]=1.[H-].[Na+].Br[CH2:18][C:19]([O:21]CC)=[O:20].[OH-].[Na+]>CN(C=O)C.C1COCC1.O>[CH3:1][C:2]1[C:12]([O:13][CH3:14])=[CH:11][C:5]2[N:6]([CH2:18][C:19]([OH:21])=[O:20])[C:7](=[O:10])[CH2:8][O:9][C:4]=2[CH:3]=1
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참가 물질

8

반응물 4

HCID 7748Ethyl bromoacetateHCID 14798Sodium HydroxideHCID 24758Sodium hydrideHCID 574186657-Methyl-6-(methyloxy)-2H-1,4-benzoxazin-3(4H)-one

생성물 1

HCID 57457164[7-Methyl-6-(methyloxy)-3-oxo-2,3-dihydro-4H-1,4-benzoxazin-4-yl]acetic acid수율 85%

시약·촉매·용매 3

HCID 962
Water
용매
HCID 6228Dimethylformamide용매
HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 7-methyl-6-(methyloxy)-2H-1,4-benzoxazin-3(4H)-one (2.13 g, 11 mmol) in DMF (20 mL) was added NaH (528 mg, 13.2 mmol) in two portions. The reaction mixture was stirred for 30 minutes at room temperature, and ethyl bromoacetate (1.22 mL, 11 mmol) was added. The reaction mixture was stirred for 3 hour until all starting material was consumed, then poured into cold water (200 mL). The precipitate was collected by filtration, washed with water, and dried in the air to afford a pale solid. This solid was dissolved in THF (22 mL) and NaOH (2.0 M, 5.5 mL) was added, and the reaction mixture was stirred at room temperature for 2 h, poured into cold water (100 mL), and extracted with EtOAc (2×100 mL). The aqueous layer was acidified with HCl (6 N) to pH˜1, extracted with EtOAc (3×100 mL). The organic extracts were combined, washed with brine, and dried (Na2SO4). The solvent was removed via rotovap to give the title compound (2.35 g, 85%) as a pale solid. MS (ES) m/e 252 [M+H]+.

후처리

  1. stirringThe reaction mixture was stirred for 3 hour until all starting material
  2. customwas consumed
  3. additionpoured into cold water (200 mL)
  4. filtrationThe precipitate was collected by filtration
  5. washwashed with water
  6. customdried in the air
  7. customto afford a pale solid
  8. stirringthe reaction mixture was stirred at room temperature for 2 h
  9. extractionextracted with EtOAc (2×100 mL)
  10. extractionextracted with EtOAc (3×100 mL)
  11. washwashed with brine
  12. dry with materialdried (Na2SO4)
  13. customThe solvent was removed via rotovap

출처 및 근거

ORD 기록
ord-7423fe59e363428a9626a2ae33415bdc
출처 데이터셋
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07749998B2

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