تفاعل #155418

ord-dc2e3fc74cd74501b2df09a9e7e7b089

معادلة التفاعل

O=Cc1ccc(O)cc1
4-hydroxybenzaldehyde
ClCCl
CH2Cl2
c1ccncc1
pyridine
CC(C)OC(=O)Cl
isopropyl chloroformate
CC(C)OC(=O)Oc1ccc(C=O)cc1
4-formylphenyl isopropyl carbonate
المردود 100.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىTo a 250 mL dry round bottom flask
  2. 2
    workup.STIRRINGAfter stirring at 0° C. for 2 hours
  3. 3
    أخرىThe aqueous layer was separated
  4. 4
    غسيلthe MTBE layer was washed
  5. 5
    تجفيفThe organic layer was dried over Na2SO4
  6. 6
    أخرىthe solvent was evaporated

الإجراء التجريبي

To a 250 mL dry round bottom flask were added 4-hydroxybenzaldehyde (4.88 g, 40.0 mmol), anhydrous CH2Cl2 (40 mL) and pyridine (4.2 mL, 52.0 mmol). The mixture was stirred in an ice-water bath, then a solution of isopropyl chloroformate in toluene (1.0 M, 48.0 mL) was added. After stirring at 0° C. for 2 hours, water (100 mL) and MTBE (300 mL) were added to the reaction mixture. The aqueous layer was separated, and the MTBE layer was washed, respectively, with cold water (80 mL), cold 5% NaOH aqueous solution (80 mL), cold water (80 mL), cold 0.5 N HCl aqueous solution (80 mL) and cold water (80 mL). The organic layer was dried over Na2SO4, and the solvent was evaporated to give 4-formylphenyl isopropyl carbonate (8.50 g) as pale yellow oil. Yield: 100%. 1H NMR (CDCl3, 300 MHz): δ=9.71 (s, 1H), 7.64 (d, J=8.4 Hz, 2H), 7.10 (d, J=8.7 Hz, 2H), 4.73 (seventet, J=6.0 Hz, 1H), 1.12 (d, J=6.3 Hz, 6H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08822435B2uspto-grants-2014_09