تفاعل #1340556

ord-64c890373e31474e8e3db64fe1117611

معادلة التفاعل

Cl
hydrochloric acid
COC(=O)CCc1cccc(C(F)(F)F)c1
3-(3-trifluoromethylphenyl)-propionic acid methyl ester
C[CH](C)[Al+][CH](C)C.[H-]
diisopropyl aluminum hydride
[Cl-].[NH4+]
ammonium chloride
O=CCCc1cccc(C(F)(F)F)c1
captioned compound
المردود 101.5%
O=CCCc1cccc(C(F)(F)F)c1
3-(3-trifluoromethylphenyl)propanal
المردود 101.5%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe mixture was stirred
  2. 2
    أخرىthe resultant was separated into an aqueous layer
  3. 3
    استخلاصThe aqueous layer was extracted with dichloromethane
  4. 4
    تجفيفdried over anhydrous sodium sulfate
  5. 5
    تركيزconcentrated under reduced pressure

الإجراء التجريبي

2.40 g of 3-(3-trifluoromethylphenyl)-propionic acid methyl ester synthesized in Step 1 was dissolved in 20 ml of dry dichloromethane. 13 ml of diisopropyl aluminum hydride solution (0.91 M) in hexane was dropped over 5 minutes at −78° C. under an argon atmosphere, and the mixture was stirred at the same temperature for 40 minutes. 50 ml of a saturated ammonium chloride aqueous solution was dropped, and then the mixture was stirred and the temperature was raised to room temperature. 20 ml of water and 5 ml of concentrated hydrochloric acid were added, and the resultant was separated into an aqueous layer and an organic layer. The aqueous layer was extracted with dichloromethane, and the extract was combined with the separated organic layer, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure to afford 2.12 g of the captioned compound as an oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08454978B2uspto-grants-2013_06