تفاعل #1121786

ord-f050e34605654ff7ae1f628ab0921947

معادلة التفاعل

O=C(CCCO)c1cncc(Br)c1
1-(5-bromo-pyridin-3-yl)-4-hydroxy-butan-1-one
O=C(CCCO)c1cncc(Br)c1
1-(5-Bromo-pyridin-3-yl)-4-hydroxy-butan-1-one
CC(=O)OI1(OC(C)=O)(OC(C)=O)OC(=O)c2ccccc21
Dess-Martin periodinane
O=CCCC(=O)c1cncc(Br)c1
4-(5-Bromo-pyridin-3-yl)-4-oxo-butyraldehyde
المردود 124.9%

المذيبات

ظروف التفاعل

درجة الحرارة
25°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىof white precipitates
  2. 2
    درجة الحرارةcooled by dry-ice-acetone bath
  3. 3
    ترشيحThe solid is filtered out and
  4. 4
    تركيزThe filtrate is concentrated
  5. 5
    workup.ADDITIONThe residue is diluted with 100 mL of ether
  6. 6
    درجة الحرارةcooled by dry-ice-acetone bath
  7. 7
    أخرىprecipitates
  8. 8
    أخرىwas removed by filtration
  9. 9
    تركيزThe filtrate is concentrated

الإجراء التجريبي

To a solution of 1-(5-bromo-pyridin-3-yl)-4-hydroxy-butan-1-one (1) (5.0 g, 20.5 mmole) in 90 mL of CH2Cl2 at 25° C., is added a solution of Dess-Martin periodinane (9.6 g, 22.5 mmole) in 70 mL of CH2Cl2 slowly. After stirring at 25° C. for 20 minutes, the reaction mixture is diluted with 200 mL of ether (a lot of white precipitates came out of the solution) and cooled by dry-ice-acetone bath. The solid is filtered out and discarded. The filtrate is concentrated. The residue is diluted with 100 mL of ether and cooled by dry-ice-acetone bath and precipitates was removed by filtration. The filtrate is concentrated to give 6.2 g of 4-(5-Bromo-pyridin-3-yl)-4-oxo-butyraldehyde (2) as a pale brown oil which turned to a pale brown solid after cooled to 0° C., without further purification for next step reaction.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08546336B2uspto-grants-2013_10