تفاعل #595332

ord-fda445e7bc364eba8c12237cc4191b13

معادلة التفاعل

O
water
O=C([O-])[O-].[K+].[K+]
potassium carbonate
OC[C@H](O)CCl.[CH2-]C(C)=O
(S)-(−)-3-chloro-1,2-propanediol acetonide
O=Cc1ccc(O)cc1
4-hydroxybenzaldehyde
CC1(C)OC[C@@H](COc2ccc(C=O)cc2)O1
4-{[(4R)-2,2-Dimethyl-1,3-dioxolan-4-yl]methoxy}benzaldehyde

المذيبات

ظروف التفاعل

درجة الحرارة
160°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصthe mixture is extracted three times with in each case 500 ml of ethyl acetate
  2. 2
    غسيلThe combined organic phases are washed in each case once with 500 ml water and 500 ml of sat. aqueous sodium chloride solution
  3. 3
    تجفيفAfter drying over magnesium sulfate
  4. 4
    أخرىthe solvent is removed on a rotary evaporator
  5. 5
    أخرىthe residue is purified by column chromatography on silica gel 60 (mobile phase gradient: ethyl acetate/petroleum ether 1:9→2:8)

الإجراء التجريبي

31.2 g (255.4 mmol) of 4-hydroxybenzaldehyde are initially charged in 400 ml of dry DMF, and 105.7 g (766.1 mmol) of potassium carbonate and 50.0 g (332.0 mmol) of (S)-(−)-3-chloro-1,2-propanediol acetonide are added at RT. The mixture is stirred at 160° C. for 16 h. 4000 ml of water are then added, and the mixture is extracted three times with in each case 500 ml of ethyl acetate. The combined organic phases are washed in each case once with 500 ml water and 500 ml of sat. aqueous sodium chloride solution. After drying over magnesium sulfate, the solvent is removed on a rotary evaporator and the residue is purified by column chromatography on silica gel 60 (mobile phase gradient: ethyl acetate/petroleum ether 1:9→2:8).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09095582B2uspto-grants-2015_08