تفاعل #1868

ord-8208d819f879448fbecf7d2aa5f1ad04

معادلة التفاعل

O
water
Nc1ccc(Cl)cc1C(O)c1ccccc1Cl
2-amino-5-chloro-α-(2-chloro phenyl)benzyl alcohol
COc1ccc(C=O)c(OC)c1
2,4-dimethoxy benzaldehyde
[BH4-].[Na+]
sodium borohydride
COc1ccc(CNc2ccc(Cl)cc2C(O)c2ccccc2Cl)c(OC)c1
5-chloro-α-(2-chlorophenyl)-2-(2,4-dimethoxybenzyl)aminobenzyl alcohol
المردود 96.1%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةcooling
  2. 2
    استخلاصfollowed by extraction with ethyl acetate (200 ml×2)
  3. 3
    غسيلThe ethyl acetate layer was washed with 1N sodium hydroxide, which
  4. 4
    تجفيفwas dried over anhydrous magnesium sulfate
  5. 5
    workup.DISTILLATIONby distilling off the solvent under reduced pressure
  6. 6
    أخرىThe residue was purified by means of a silica gel column chromatography (hexane:ethyl acetate=5:1)

الإجراء التجريبي

To a solution of 2-amino-5-chloro-α-(2-chloro phenyl)benzyl alcohol (5.0 g) and 2,4-dimethoxy benzaldehyde (3.72 g) in acetic acid (50 ml) was added, under ice-cooling, sodium borohydride (0.94 g). The mixture was stirred for one hour at room temperature, which was poured into water (200 ml), followed by extraction with ethyl acetate (200 ml×2). The ethyl acetate layer was washed with 1N sodium hydroxide, which was dried over anhydrous magnesium sulfate, followed by distilling off the solvent under reduced pressure. The residue was purified by means of a silica gel column chromatography (hexane:ethyl acetate=5:1) to give 5-chloro-α-(2-chlorophenyl)-2-(2,4-dimethoxybenzyl)aminobenzyl alcohol (7.5 g) as an oily product.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05726306uspto-grants-1998_03