تفاعل #1994296

ord-99653acb62be4fa7bc5b3a51f1f9ce0e

معادلة التفاعل

O=Cc1ccc(Cl)cc1F
4-chloro-2-fluorobenzaldehyde
[Na+].[OH-]
sodium hydroxide
CC(C)=O
acetone
ClCCl
dichloromethane
CC(=O)/C=C/c1ccc(Cl)cc1F
4-(4-chloro-2-fluorophenyl)-3-buten-2-one
المردود 76.0%
CC(=O)/C=C/c1ccc(Cl)cc1F
(E)-4-(4-chloro-2-fluorophenyl)-but-3-en-2-one
المردود 76.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added
  2. 2
    أخرىThe aqueous layer was separated
  3. 3
    استخلاصextracted with CH2Cl2 (100 mL)
  4. 4
    غسيلthe combined organic extracts were washed with brine
  5. 5
    تجفيفdried over magnesium sulfate (MgSO4)
  6. 6
    أخرىSolvent removal
  7. 7
    workup.DISTILLATIONfollowed by Kugelrohr distillation

الإجراء التجريبي

To a mechanically stirred solution of 4-chloro-2-fluorobenzaldehyde (23.8 grams (g), 0.15 mole (mol)) in acetone (100 milliliters (mL)) at room temperature was added over 20 minutes (min) a solution of sodium hydroxide (NaOH, 6.6 g, 0.165 mol) in water (H2O, 400 mL). After stirring the reaction mixture overnight, dichloromethane (CH2Cl2, 100 mL) was added. The aqueous layer was separated and extracted with CH2Cl2 (100 mL), and the combined organic extracts were washed with brine and dried over magnesium sulfate (MgSO4). Solvent removal followed by Kugelrohr distillation gave 4-(4-chloro-2-fluorophenyl)-3-buten-2-one (1; 22.5 g, 76%) as a colorless liquid, which solidified upon standing: by 70-80° C., 0.1 mmHg (13.33 pascals (Pa)); 1H NMR (400 MHz, CDCl3) δ 7.59 (d, J=16.5 Hz, 1H), 7.50 (t, J=8.1 Hz, 1H), 7.22-7.12 (m, 2H), 6.76 (d, J=16.5 Hz, 1H), 2.39 (s, 3H); HRMS-ESI (m/z): calcd for C10H8ClFO, 198.024. found 198.025.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08598086B2uspto-grants-2013_12