تفاعل #1687655

ord-ad4abfbcf9ae429c9f79a37c477e5d63

معادلة التفاعل

O=C1c2ccc(O)cc2C(=O)c2ccc(O)cc21
2,6-dihydroxyanthraquinone
CCOP(=O)(CCCCBr)OCC
diethyl(4-bromobutyl)phosphonate
O=C([O-])[O-].[K+].[K+]
K2CO3
O=C1c2ccc(OCCCCP(=O)(O)O)cc2C(=O)c2ccc(OCCCCP(=O)(O)O)cc21
2,6-Bis (4-phosphonobutyloxy)-anthraquinone

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصThe solution was extracted with CH2Cl2
  2. 2
    تجفيفThe CH2Cl2 solution was dried
  3. 3
    أخرىleaving a yellow solid
  4. 4
    أخرىThe ester was purified by column chromatography
  5. 5
    workup.ADDITIONfollowed by addition of water
  6. 6
    غسيلThe bisphosphonic acid derivative was washed with CH2Cl2
  7. 7
    ترشيحfiltered
  8. 8
    أخرىcollected

الإجراء التجريبي

2,6-dihydroxyanthraquinone (1.19 g, 4.98 mmol) and diethyl(4-bromobutyl)phosphonate (3.0 g, 10 mmol) were heated at 60 ° C. in 5 ml DMF in the presence of 0.8 g of K2CO3 for 72 hours. The solution was extracted with CH2Cl2. The CH2Cl2 solution was dried, leaving a yellow solid. The ester was purified by column chromatography. The bisphosphonate ester was converted to the acid by overnight stirring with 4-fold excess of bromotrimethylsilane in dry dichloromethane followed by addition of water. The bisphosphonic acid derivative was washed with CH2Cl2, filtered and collected.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05976486uspto-grants-1999_11