تفاعل #684957

ord-c33085f8c1744614a8e04291c2341459

معادلة التفاعل

O
water
CCN(C(C)C)C(C)C
N,N-diisopropylethylamine
COCCl
chloromethyl methyl ether
O=Cc1ccc(OCc2ccccc2)cc1O
4-benzyloxy-2-hydroxybenzaldehyde
CCN(C(C)C)C(C)C
N,N-diisopropylethylamine
COCCl
chloromethyl methyl ether
COCOc1cc(OCc2ccccc2)ccc1C=O
title compound
COCOc1cc(OCc2ccccc2)ccc1C=O
4-Benzyloxy-2-(methoxymethoxy)benzaldehyde

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةheated
  2. 2
    درجة الحرارةunder reflux for 19 hours
  3. 3
    workup.STIRRINGthe resulting mixture was stirred
  4. 4
    درجة الحرارةheated
  5. 5
    درجة الحرارةunder reflux for another 10 hours
  6. 6
    استخلاصthe reaction mixture was extracted with ethyl acetate
  7. 7
    غسيلwashed with a saturated aqueous ammonium chloride solution and saturated brine
  8. 8
    تجفيفdried over anhydrous magnesium sulfate
  9. 9
    ترشيحfiltered through silica gel and alumina
  10. 10
    تركيزThe filtrate was concentrated under reduced pressure

الإجراء التجريبي

N,N-diisopropylethylamine (1.98 ml) and chloromethyl methyl ether (0.76 ml) were added to a solution of 4-benzyloxy-2-hydroxybenzaldehyde (2071 mg) in tetrahydrofuran (30 ml), and this reaction mixture was stirred and heated under reflux for 19 hours. N,N-diisopropylethylamine (2.7 ml) and chloromethyl methyl ether (1.04 ml) were further added, and the resulting mixture was stirred and heated under reflux for another 10 hours. After water was added, the reaction mixture was extracted with ethyl acetate, washed with a saturated aqueous ammonium chloride solution and saturated brine, dried over anhydrous magnesium sulfate, then filtered through silica gel and alumina. The filtrate was concentrated under reduced pressure to give the title compound (2470 mg). This compound was used in the following reaction without further purification.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07897387B2uspto-grants-2011_03