تفاعل #1121737

ord-89a3d57a636040e6a207f111233d7730

معادلة التفاعل

CCCCC/C=C\C/C=C\CCCCCCCCOS(C)(=O)=O
linoleyl methanesulfonate
Cc1ccccc1
toluene
CN(C)CC(O)CO
3-(dimethylamino)-1,2-propanediol
[H-].[Na+]
NaH
Cc1ccccc1
toluene
Cc1ccccc1
toluene
CCCCC/C=C\C/C=C\CCCCCCCCOCCC(O)CN(C)C
1-(dimethylamino)-4-((9Z,12Z)-octadeca-9,12-dienyloxy)butan-2-ol

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe reaction was then stirred for 18 hours at 90° C
  2. 2
    أخرىquenched by the slow addition of ethanol (10 mL)
  3. 3
    تركيزThe mixture was concentrated
  4. 4
    استخلاصextracted three times with EtOAc (30 mL)
  5. 5
    غسيلThe combined organic extracts were washed with deionized water (20 mL)
  6. 6
    تجفيفdried (MgSO4)
  7. 7
    ترشيحfiltered
  8. 8
    تركيزconcentrated
  9. 9
    أخرىChromatographic purification of the residue (0-5% MeOH in chloroform)

الإجراء التجريبي

A toluene (10 mL) solution of 3-(dimethylamino)-1,2-propanediol (98%, 1.00 g, 8.39 mmol, 1.0 equiv)) was carefully added dropwise to a toluene suspension (5 mL) of NaH (60%, 0.34 g, 8.39 mmol, 1.0 equiv) at 0° C. under argon and the resultant was stirred for 15 minutes. A toluene solution (5 mL) of linoleyl methanesulfonate (2.87 g, 8.39 mmol, 1.0 equiv) was added dropwise to the stirring mixture and the reaction was then stirred for 18 hours at 90° C. The mixture was then cooled to room temperature and quenched by the slow addition of ethanol (10 mL). The mixture was concentrated and the residue was taken up with deionized water (20 mL) and extracted three times with EtOAc (30 mL). The combined organic extracts were washed with deionized water (20 mL), dried (MgSO4), filtered, and concentrated. Chromatographic purification of the residue (0-5% MeOH in chloroform) provided 1-(dimethylamino)-4-((9Z,12Z)-octadeca-9,12-dienyloxy)butan-2-ol, a thick, clear oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08545876B1uspto-grants-2013_10