تفاعل #9878

ord-bbd607b812354346904cf9218fbabf16

معادلة التفاعل

Cl
HCl
O=C(O)C(Cc1ccccc1)C(=O)O
benzylmalonic acid
C=O
paraformaldehyde
CCNCC
diethylamine
C=C(Cc1ccccc1)C(=O)O
compound 17
المردود 90.0%
C=C(Cc1ccccc1)C(=O)O
2-methylene-3-phenylpropanoic acid
المردود 90.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe reaction temperature below 20° C. (see FIG. 6)
  2. 2
    درجة الحرارةThe reaction was then warmed
  3. 3
    درجة الحرارةto reflux for 90 min
  4. 4
    درجة الحرارةcooled again on ice
  5. 5
    أخرىthe reaction temperature below 10° C
  6. 6
    أخرىThe phases were then separated
  7. 7
    غسيلThe organic layer was washed with brine (100 mL)
  8. 8
    تجفيفdried over sodium sulfate
  9. 9
    ترشيحfiltered
  10. 10
    تركيزthe filtrate concentrated under vacuum

الإجراء التجريبي

A solution of benzylmalonic acid (20.0 g, 0.103 mol, 1 eq) and paraformaldehyde (4.94 g, 0.164 mol, 1.6 eq) in ethyl acetate (150 mL) was cooled (0° C.) and treated with diethylamine (10.65 mL, 0.103 mol, 1 eq) drop wise, keeping the reaction temperature below 20° C. (see FIG. 6). The reaction was then warmed to reflux for 90 min and cooled again on ice. The homogeneous solution was treated with water (20 mL) and concentrated aqueous HCl (12N) (9.0 mL, 0.108 mol) drop wise, keeping the reaction temperature below 10° C. The phases were then separated. The organic layer was washed with brine (100 mL), dried over sodium sulfate, filtered, and the filtrate concentrated under vacuum giving compound 17 as a white solid (15 g, 90%). Rf 0.46 (hexane/EtOAc=7:3). 1H NMR (300 MHz, CDCl3) δ 7.28 (m, 5H), 6.42 (s, 1H), 5.62 (s, 1H), 3.67 (s, 2H). [M−H]− 161.0: tR=2.53 min; purity: 99%.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07091354B2uspto-grants-2006_08