반응 #1726662

ord-cfd10bd3bcdd438b8b4b53fa7c79eee2

반응 방정식

CC1(C)C(=O)N(I)C(=O)N1I
1,3-diiodo-5,5-dimethylimidazolidine-2,4-dione
c1ccc(-c2c3ccccc3cc3ccccc23)cc1
9-phenylanthracene
CC(=O)O
acetic acid
O
water
c1ccc(-c2c3ccccc3cc3ccccc23)cc1
9-phenylanthracene
Ic1c2ccccc2c(-c2ccccc2)c2ccccc12
yellow solid
수율 117.3%
Ic1c2ccccc2c(-c2ccccc2)c2ccccc12
9-iodo-10-phenylanthracene
수율 117.3%

반응 조건

온도
70°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척This mixture was washed with water twice
  2. 2
    추출the aqueous layer was extracted with chloroform
  3. 3
    세척washed with a saturated saline
  4. 4
    건조the organic layer was dried with magnesium sulfate
  5. 5
    여과filtered
  6. 6
    농축the obtained filtrate was concentrated
  7. 7
    기타to give a brown solid
  8. 8
    세척This solid was washed with hexane

실험 절차

Into a 500 mL Erlenmeyer flask was put 4.5 g (18 mmol) of 9-phenylanthracene. Then 200 mL of acetic acid was added to the flask, followed by heating to 70° C., and 9-phenylanthracene was dissolved therein. Into this solution, 5.2 g (13 mmol) of 1,3-diiodo-5,5-dimethylimidazolidine-2,4-dione (abbreviation: DIH) was added. This solution was stirred in air at 70° C. for 3 hours. After the stirring, about 100 mL of water and about 200 mL of chloroform were added to this solution. This mixture was washed with water twice, and the aqueous layer was extracted with chloroform. The extracted solution was combined with the organic layer and washed with a saturated saline, and then the organic layer was dried with magnesium sulfate. This mixture was gravity filtered, and the obtained filtrate was concentrated to give a brown solid. This solid was washed with hexane to give 5.8 g of a yellow solid, which was the object of the synthesis, in a yield of 86%.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08110122B2uspto-grants-2012_02