تفاعل #2446103

ord-0aa175e9ac194f15a1226de436e04c87

معادلة التفاعل

O=C(Cl)C12CC3CC(CC(C3)C1)C2
1-adamantanecarbonyl chloride
CC(C)[N-]C(C)C.[Li+]
lithium diisopropylamide
C=C(C)C(N)=O
methacrylamide
COC(C)(C)C
t-butylmethylether
C=C(C)C(N)=O.O=C(O)C12CC3CC(CC(C3)C1)C2
1-adamantanecarboxylic acid methacrylamide

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىat 5° C.
  2. 2
    workup.ADDITIONtherein was added
  3. 3
    workup.STIRRINGby stirring at 5° C. for 18 hours
  4. 4
    workup.ADDITIONwere added
  5. 5
    غسيلby washing with a 1 wt % aqueous hydrochloric acid solution and pure water, and concentration under reduced pressure
  6. 6
    workup.ADDITIONn-hexane was added to the obtained solution, and crystallization
  7. 7
    أخرىwas conducted at 5° C.
  8. 8
    ترشيحfollowed by filtration
  9. 9
    أخرىThe obtained solid was dried under reduced pressure

الإجراء التجريبي

90.0 g of methacrylamide was dissolved in 1,350 g of tetrahydrofuran (THF), and 944 mL of a 1.12 mol/L lithium diisopropylamide (LiDA) solution was dropwise added thereto at 5° C., followed by stirring for 10 minutes. Subsequently, 900 g of THF having 231.1 g of 1-adamantanecarbonyl chloride dissolved therein was added thereto, followed by stirring at 5° C. for 18 hours. After completion of the reaction, THF and t-butylmethylether (TBME) were added thereto, followed by washing with a 1 wt % aqueous hydrochloric acid solution and pure water, and concentration under reduced pressure. n-hexane was added to the obtained solution, and crystallization was conducted at 5° C., followed by filtration. The obtained solid was dried under reduced pressure, thereby obtaining 194.4 g of 1-adamantanecarboxylic acid methacrylamide (compound (51)).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08685620B2uspto-grants-2014_04