반응 #806240

ord-91f846d116934ed5ba34016083d90089

반응 방정식

CCCCCCC(CO)OO
2-hydroperoxy-1-hydroxyoctane
OO
hydrogen peroxide
CC(C)(C)O
tert-butanol
C=CCCCCCC
1-octene
CCCCCCC(O)COO
1-hydroperoxy-2-hydroxyoctane
수율 42.0%

반응 조건

온도
50°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타To a 50 mL flask equipped with a magnetic stirrer
  2. 2
    기타a refluxing condensing tube
  3. 3
    기타to react these materials
  4. 4
    기타To the resulting reaction mixture
  5. 5
    workup.STIRRINGthe mixture was stirred

실험 절차

To a 50 mL flask equipped with a magnetic stirrer and a refluxing condensing tube were added 300 mg of the tungsten-containing mesoporous silicate prepared in Example 2, 760 mg of 60% by weight aqueous hydrogen peroxide solution, 3 g of tert-butanol and 500 mg of 1-octene, and the mixture was stirred and maintained at an inner temperature of 50° C. for 16 hours to react these materials. To the resulting reaction mixture was added 5 g of methyl tert-butyl ether, and the mixture was stirred, and allowed to stand. The supernatant organic layer was analyzed by LC, and it was found that 2-hydroperoxy-1-hydroxyoctane and 1-hydroperoxy-2-hydroxyoctane were produced. When the organic layer was analyzed by GC, 2-hydroperoxy-1-hydroxyoctane and 1-hydroperoxy-2-hydroxyoctane were thermally decomposed at an injection inlet, and detected as 1-heptanal. Then, the yield of 1-heptanal was determined by GC analysis (internal standard method), and this was regarded as the yield of 2-hydroperoxy-1-hydroxyoctane and 1-hydroperoxy-2-hydroxyoctane. Yield: 42%

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07132092B2uspto-grants-2006_11