تفاعل #1553

ord-febb9432bc444d1b8660781f308ba31e

معادلة التفاعل

CCOCC
ether
O
water
C#CCn1c(-c2cccc(C3OCCO3)c2)nc(CC)c(CC)c1=O
5,6-diethyl-2-[3-(2-dioxolanyl)phenyl]-3-propargyl-4(3H)-pyrimidinone
Cl
hydrochloric acid
C#CCn1c(-c2cccc(C=O)c2)nc(CC)c(CC)c1=O
5,6-diethyl-2-(3-formylphenyl)-3-propargyl-4(3H)-pyrimidinone
المردود 86.4%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwere added to the reaction mixture
  2. 2
    أخرىThe layers were separated
  3. 3
    استخلاصthe aqueous layer was extracted twice with 50 mL of ether
  4. 4
    تجفيفdried over MgSO4
  5. 5
    تركيزconcentrated

الإجراء التجريبي

To a solution of 2.3 g (6.8 mmol) of 5,6-diethyl-2-[3-(2-dioxolanyl)phenyl]-3-propargyl-4(3H)-pyrimidinone in 1 mL of ethyl acetate was added 50 mL of 6M hydrochloric acid and the mixture was stirred for 4 hours. The reaction was followed by gas chromatography and TLC(20% ethyl acetate in hexane). Upon completion of reaction, 75 mL of ether and 150 mL of water were added to the reaction mixture. The layers were separated and the aqueous layer was extracted twice with 50 mL of ether. The organic layers were combined, dried over MgSO4 and concentrated to yield 1.73 g of 5,6-diethyl-2-(3-formylphenyl)-3-propargyl-4(3H)-pyrimidinone (Compound 69) as a yellow oil (86%), which solidified on standing. Mp.=82°-86° C. 1H-NMR (CDCl3) δ 1.25(6H,m), 2.4(1H,t), 2.65(4H,q), 4.6(2H,d), 7.7(1H,t), 8.05(2H,m), 8.25(1H,s), 10.15(1H,s).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05726124uspto-grants-1998_03