反应 #453534

ord-4646b01659524c8590fa560b9eb12837

反应方程式

CC(C)OC(=O)[N+](=[N-])C(=O)OC(C)C
diisopropyldiazodicarboxylate
O=C1c2ccccc2OCN1CCO
3-(2-hydroxyethyl)-4-oxo-3,4-dihydro-1,3-benzoxazine
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
CCOC(=O)C(Cc1ccc(O)cc1)OCC
(+)-ethyl 2-ethoxy-3-(4-hydroxyphenyl)propanoate
CCOC(=O)C(Cc1ccc(OCCN2COc3ccccc3C2=O)cc1)OCC
title compound
收率 76.0%
CCOC(=O)C(Cc1ccc(OCCN2COc3ccccc3C2=O)cc1)OCC
(+)-Ethyl 2-ethoxy-3-[4-[2-[4-oxo-3,4-dihydro-1,3-benzoxazin-3-yl]ethoxy]phenyl]propanoate
收率 76.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.STIRRINGstirred for further 40 h
  2. 2
    萃取extracted with ethyl acetate (3×10 mL)
  3. 3
    洗涤The combined organic extracts were washed with brine
  4. 4
    干燥dried over anhydrous Na2SO4
  5. 5
    浓缩concentrated
  6. 6
    其他The residue was chromatographed on silica gel using a gradient of 5-15% ethyl acetate in pet ether as eluent

实验过程

To a stirred mixture of 3-(2-hydroxyethyl)-4-oxo-3,4-dihydro-1,3-benzoxazine (325 mg, 1.68 mmol) and triphenylphosphine (660 mg, 2.52 mmol) in toluene (10 mL) was added a solution of (+)-ethyl 2-ethoxy-3-(4-hydroxyphenyl)propanoate (400 mg, 1.68 mmol) at 25° C. and stirred for 10 min. To the reaction mixture was added diisopropyldiazodicarboxylate (0.5 mL, 2.52 mmol) at 25-30° C. and stirred for further 40 h. Water was added to the reaction mixture and extracted with ethyl acetate (3×10 mL). The combined organic extracts were washed with brine, dried over anhydrous Na2SO4 and concentrated. The residue was chromatographed on silica gel using a gradient of 5-15% ethyl acetate in pet ether as eluent to afford the title compound (527 mg, 76%): mp 76-78° C.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06130214uspto-grants-2000_10